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

dbVar

Database of genomic structural variation

nsv5543775

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Byrska-Bishop et al. 2022

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: 255 SVs from 19 studies. See in: genome view

Submitted genomic87,538,090-87,538,090

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5543775	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	87,538,090	87,538,090
nsv5543775	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	86,793,093	86,793,093

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17741274	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17741274	Submitted genomic		NC_000023.11:g.875 38090_87538091ins5 48	GRCh38 (hg38)		NC_000023.11	ChrX	87,538,090	87,538,090
nssv17741274	Remapped	Perfect	NC_000023.10:g.867 93093_86793094ins5 48	GRCh37.p13	First Pass	NC_000023.10	ChrX	86,793,093	86,793,093

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17741274	<0.001	1	4004

You are here: NCBI