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dbVar

Database of genomic structural variation

nsv5720951

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 L1 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: 163 SVs from 18 studies. See in: genome view

Submitted genomic21,441,685-21,441,685

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5720951	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	21,441,685	21,441,685
nsv5720951	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	19,021,646	19,021,646

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17242503	line1 insertion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17242503	Submitted genomic		NC_000018.10:g.214 41685_21441686ins1 142	GRCh38 (hg38)		NC_000018.10	Chr18	21,441,685	21,441,685
nssv17242503	Remapped	Perfect	NC_000018.9:g.1902 1646_19021647ins11 42	GRCh37.p13	First Pass	NC_000018.9	Chr18	19,021,646	19,021,646

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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