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dbVar

Database of genomic structural variation

nsv2768202

Organism: Homo sapiens

Study:nstd125 (Wills et al. 2016)
Variant Type:complex substitution
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:155,750,813

Publication(s):Wills et al. 2016

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: 217754 SVs from 118 studies. See in: genome view

Remapped(Score: Good):253,254-156,004,066

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv2768202	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	253,254	156,004,066
nsv2768202	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	169,921	155,233,731

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Copy number	Other Calls in this Sample and Study
nssv13638306	complex substitution	20	SNP array	SNP genotyping analysis	3	nssv13638304, nssv13638305
nssv13638307	complex substitution	27	SNP array	SNP genotyping analysis	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv13638306	Remapped	Good	GRCh38.p12	First Pass	NC_000023.11	ChrX	253,254	156,004,066
nssv13638307	Remapped	Good	GRCh38.p12	First Pass	NC_000023.11	ChrX	253,254	156,004,066
nssv13638306	Submitted genomic		GRCh37 (hg19)		NC_000023.10	ChrX	169,921	155,233,731
nssv13638307	Submitted genomic		GRCh37 (hg19)		NC_000023.10	ChrX	169,921	155,233,731

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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