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

dbVar

Database of genomic structural variation

nsv5605679

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

Submitted genomic87,663,423-87,663,423

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5605679	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	87,663,423	87,663,423
nsv5605679	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	86,918,423	86,918,423

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17168544	insertion	SAMN00249890	Sequencing	Sequence alignment	1,169

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17168544	Submitted genomic		NC_000023.11:g.876 63423_87663424ins3 35	GRCh38 (hg38)		NC_000023.11	ChrX	87,663,423	87,663,423
nssv17168544	Remapped	Perfect	NC_000023.10:g.869 18423_86918424ins3 35	GRCh37.p13	First Pass	NC_000023.10	ChrX	86,918,423	86,918,423

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