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dbVar

Database of genomic structural variation

nsv6627098

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:11,313

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: 127 SVs from 34 studies. See in: genome view

Remapped(Score: Perfect):33,066,268-33,077,580

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6627098	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000022.11	Chr22	33,066,268	33,077,580
nsv6627098	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000022.10	Chr22	33,462,254	33,473,566

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18307598	deletion	OSC6766	SNP array	Probe signal intensity	10
nssv18318428	deletion	OSC8524	SNP array	Probe signal intensity	8

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18307598	Remapped	Perfect	NC_000022.11:g.(?_ 33066268)_(3307758 0_?)del	GRCh38.p12	First Pass	NC_000022.11	Chr22	33,066,268	33,077,580
nssv18318428	Remapped	Perfect	NC_000022.11:g.(?_ 33066268)_(3307758 0_?)del	GRCh38.p12	First Pass	NC_000022.11	Chr22	33,066,268	33,077,580
nssv18307598	Submitted genomic		NC_000022.10:g.(?_ 33462254)_(3347356 6_?)del	GRCh37 (hg19)		NC_000022.10	Chr22	33,462,254	33,473,566
nssv18318428	Submitted genomic		NC_000022.10:g.(?_ 33462254)_(3347356 6_?)del	GRCh37 (hg19)		NC_000022.10	Chr22	33,462,254	33,473,566

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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