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dbVar

Database of genomic structural variation

nsv6635899

Organism: Homo sapiens

Study:nstd227 (Kikas et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:4
Validation:Not tested
Clinical Assertions: No
Region Size:93,386

Publication(s):Kikas et al. 2023

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 1341 SVs from 103 studies. See in: genome view

Remapped(Score: Perfect):31,392,478-31,485,863

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv6635899	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	31,392,478	31,485,863
nsv6635899	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	31,360,255	31,453,640

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18328567	duplication	SNP array	Probe signal intensity
nssv18328568	duplication	SNP array	Probe signal intensity
nssv18328569	duplication	SNP array	Probe signal intensity
nssv18328570	duplication	SNP array	Probe signal intensity

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv18328567	Remapped	Perfect	NC_000006.12:g.(31 392478_?)_(?_31485 863)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	31,392,478	31,485,863
nssv18328568	Remapped	Perfect	NC_000006.12:g.(31 392478_?)_(?_31485 863)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	31,392,478	31,485,863
nssv18328569	Remapped	Perfect	NC_000006.12:g.(31 392478_?)_(?_31485 863)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	31,392,478	31,485,863
nssv18328570	Remapped	Perfect	NC_000006.12:g.(31 392478_?)_(?_31485 863)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	31,392,478	31,485,863
nssv18328567	Submitted genomic		NC_000006.11:g.(31 360255_?)_(?_31453 640)dup	GRCh37 (hg19)		NC_000006.11	Chr6	31,360,255	31,453,640
nssv18328568	Submitted genomic		NC_000006.11:g.(31 360255_?)_(?_31453 640)dup	GRCh37 (hg19)		NC_000006.11	Chr6	31,360,255	31,453,640
nssv18328569	Submitted genomic		NC_000006.11:g.(31 360255_?)_(?_31453 640)dup	GRCh37 (hg19)		NC_000006.11	Chr6	31,360,255	31,453,640
nssv18328570	Submitted genomic		NC_000006.11:g.(31 360255_?)_(?_31453 640)dup	GRCh37 (hg19)		NC_000006.11	Chr6	31,360,255	31,453,640

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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