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dbVar

Database of genomic structural variation

nsv6314791

Organism: Homo sapiens

Study:nstd220 (Chen et al. 2022)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,430,553

Publication(s):Chen et al. 2022

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: 4507 SVs from 111 studies. See in: genome view

Remapped(Score: Perfect):14,223,054-15,653,606

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv6314791	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	14,223,054	15,653,606
nsv6314791	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	14,126,371	15,556,920

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17976216	copy number gain	Sequencing	Read depth

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv17976216	Remapped	Perfect	NC_000017.11:g.(14 223054_?)_(?_15653 606)dup	GRCh38.p12	First Pass	NC_000017.11	Chr17	14,223,054	15,653,606
nssv17976216	Submitted genomic		NC_000017.10:g.(14 126371_?)_(?_15556 920)dup	GRCh37 (hg19)		NC_000017.10	Chr17	14,126,371	15,556,920

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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