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dbVar

Database of genomic structural variation

nsv5703869

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: 105 SVs from 21 studies. See in: genome view

Submitted genomic116,171,578-116,171,578

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5703869	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	116,171,578	116,171,578
nsv5703869	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	117,931,090	117,931,090

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17221431	alu insertion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17221431	Submitted genomic		NC_000010.11:g.116 171578_116171579in s278	GRCh38 (hg38)		NC_000010.11	Chr10	116,171,578	116,171,578
nssv17221431	Remapped	Perfect	NC_000010.10:g.117 931090_117931091in s278	GRCh37.p13	First Pass	NC_000010.10	Chr10	117,931,090	117,931,090

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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