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dbVar

Database of genomic structural variation

nsv5724015

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

Submitted genomic21,316,189-21,316,189

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5724015	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	21,316,189	21,316,189
nsv5724015	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	18,896,150	18,896,150

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17248495	line1 insertion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17248495	Submitted genomic		NC_000018.10:g.213 16189_21316190ins9 79	GRCh38 (hg38)		NC_000018.10	Chr18	21,316,189	21,316,189
nssv17248495	Remapped	Perfect	NC_000018.9:g.1889 6150_18896151ins97 9	GRCh37.p13	First Pass	NC_000018.9	Chr18	18,896,150	18,896,150

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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