Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv5615122

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: 500 SVs from 47 studies. See in: genome view

Submitted genomic135,828,773-135,828,773

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5615122	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	135,828,773	135,828,773
nsv5615122	Remapped	Perfect	GRCh37.p13	PATCHES	First Pass	NW_004070887.1	ChrX\|NW_00 4070887.1	759,916	759,916

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17165576	insertion	HG03065	Sequencing	Sequence alignment	3,836

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17165576	Submitted genomic		NC_000023.11:g.135 828773_135828774in s61	GRCh38 (hg38)		NC_000023.11	ChrX	135,828,773	135,828,773
nssv17165576	Remapped	Perfect	NW_004070887.1:g.7 59916_759917ins61	GRCh37.p13	First Pass	NW_004070887.1	ChrX\|NW_00 4070887.1	759,916	759,916

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.

You are here: NCBI