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dbVar

Database of genomic structural variation

nsv4369186

Organism: Homo sapiens

Study:nstd173 (Zarrei et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:146,647

Publication(s):Zarrei et al. 2019

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: 587 SVs from 43 studies. See in: genome view

Remapped(Score: Perfect):99,458,496-99,605,142

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4369186	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	99,458,496	99,605,142
nsv4369186	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	98,713,494	98,860,140

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15611661	copy number loss	1-0653-001	SNP array	Genotyping	19
nssv15611760	copy number loss	1-0653-006	SNP array	Genotyping	12

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15611661	Remapped	Perfect	NC_000023.11:g.(?_ 99458496)_(9960514 2_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	99,458,496	99,605,142
nssv15611760	Remapped	Perfect	NC_000023.11:g.(?_ 99458496)_(9960514 2_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	99,458,496	99,605,142
nssv15611661	Submitted genomic		NC_000023.10:g.(?_ 98713494)_(9886014 0_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	98,713,494	98,860,140
nssv15611760	Submitted genomic		NC_000023.10:g.(?_ 98713494)_(9886014 0_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	98,713,494	98,860,140

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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