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dbVar

Database of genomic structural variation

nsv5611639

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert et al. 2021

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: 423 SVs from 24 studies. See in: genome view

Submitted genomic110,689,951-110,689,951

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5611639	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	110,689,951	110,689,951
nsv5611639	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	109,933,179	109,933,179

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17164706	insertion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17164706	Submitted genomic		NC_000023.11:g.110 689951_110689952in s51	GRCh38 (hg38)		NC_000023.11	ChrX	110,689,951	110,689,951
nssv17164706	Remapped	Perfect	NC_000023.10:g.109 933179_109933180in s51	GRCh37.p13	First Pass	NC_000023.10	ChrX	109,933,179	109,933,179

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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