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

dbVar

Database of genomic structural variation

nsv5710138

Organism: Homo sapiens

Study:nstd211 (Chuang et al. 2021)
Variant Type:mobile element insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Description:Insertion of a Alu mobile element relative to the reference
Publication(s):Chuang 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: 91 SVs from 19 studies. See in: genome view

Submitted genomic82,856,262-82,856,262

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5710138	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	82,856,262	82,856,262
nsv5710138	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	82,567,304	82,567,304

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17190566	alu insertion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17190566	Submitted genomic		NC_000011.10:g.828 56262_82856263ins2 79	GRCh38 (hg38)		NC_000011.10	Chr11	82,856,262	82,856,262
nssv17190566	Remapped	Perfect	NC_000011.9:g.8256 7304_82567305ins27 9	GRCh37.p13	First Pass	NC_000011.9	Chr11	82,567,304	82,567,304

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