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dbVar

Database of genomic structural variation

nsv6628644

Organism: Homo sapiens

Study:nstd224 (Zarrei et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:255,140

Publication(s):Zarrei 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: 891 SVs from 67 studies. See in: genome view

Remapped(Score: Perfect):142,106,082-142,361,221

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6628644	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	142,106,082	142,361,221
nsv6628644	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	141,824,924	142,080,063

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18301851	duplication	OSC5795	SNP array	Probe signal intensity	9
nssv18319245	duplication	OSC8650	SNP array	Probe signal intensity	11

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18301851	Remapped	Perfect	NC_000003.12:g.(?_ 142106082)_(142361 221_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	142,106,082	142,361,221
nssv18319245	Remapped	Perfect	NC_000003.12:g.(?_ 142106082)_(142361 221_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	142,106,082	142,361,221
nssv18301851	Submitted genomic		NC_000003.11:g.(?_ 141824924)_(142080 063_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	141,824,924	142,080,063
nssv18319245	Submitted genomic		NC_000003.11:g.(?_ 141824924)_(142080 063_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	141,824,924	142,080,063

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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