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dbVar

Database of genomic structural variation

nsv5728965

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 SVA 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: 96 SVs from 21 studies. See in: genome view

Submitted genomic45,718,942-45,718,942

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5728965	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	45,718,942	45,718,942
nsv5728965	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	46,222,200	46,222,200

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17241042	sva insertion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17241042	Submitted genomic		NC_000019.10:g.457 18942_45718943ins1 240	GRCh38 (hg38)		NC_000019.10	Chr19	45,718,942	45,718,942
nssv17241042	Remapped	Perfect	NC_000019.9:g.4622 2200_46222201ins12 40	GRCh37.p13	First Pass	NC_000019.9	Chr19	46,222,200	46,222,200

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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