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dbVar

Database of genomic structural variation

nsv5729980

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: 102 SVs from 28 studies. See in: genome view

Submitted genomic64,978,270-64,978,270

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5729980	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	64,978,270	64,978,270
nsv5729980	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	64,963,945	64,963,945

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17248396	line1 insertion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17248396	Submitted genomic		NC_000003.12:g.649 78270_64978271ins3 649	GRCh38 (hg38)		NC_000003.12	Chr3	64,978,270	64,978,270
nssv17248396	Remapped	Perfect	NC_000003.11:g.649 63945_64963946ins3 649	GRCh37.p13	First Pass	NC_000003.11	Chr3	64,963,945	64,963,945

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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