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dbVar

Database of genomic structural variation

nsv5696641

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: 303 SVs from 30 studies. See in: genome view

Submitted genomic17,905,443-17,905,443

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5696641	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	17,905,443	17,905,443
nsv5696641	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	17,762,952	17,762,952

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17183919	alu insertion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17183919	Submitted genomic		NC_000008.11:g.179 05443_17905444ins2 81	GRCh38 (hg38)		NC_000008.11	Chr8	17,905,443	17,905,443
nssv17183919	Remapped	Perfect	NC_000008.10:g.177 62952_17762953ins2 81	GRCh37.p13	First Pass	NC_000008.10	Chr8	17,762,952	17,762,952

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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