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dbVar

Database of genomic structural variation

nsv5718845

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: 267 SVs from 37 studies. See in: genome view

Submitted genomic77,945,294-77,945,294

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5718845	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	77,945,294	77,945,294
nsv5718845	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	77,979,191	77,979,191

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17235687	line1 insertion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17235687	Submitted genomic		NC_000016.10:g.779 45294_77945295ins2 149	GRCh38 (hg38)		NC_000016.10	Chr16	77,945,294	77,945,294
nssv17235687	Remapped	Perfect	NC_000016.9:g.7797 9191_77979192ins21 49	GRCh37.p13	First Pass	NC_000016.9	Chr16	77,979,191	77,979,191

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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