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dbVar

Database of genomic structural variation

nsv5698649

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 Alu 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: 97 SVs from 20 studies. See in: genome view

Submitted genomic54,870,335-54,870,335

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5698649	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	54,870,335	54,870,335
nsv5698649	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	55,337,053	55,337,053

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17220717	alu insertion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17220717	Submitted genomic		NC_000014.9:g.5487 0335_54870336ins27 9	GRCh38 (hg38)		NC_000014.9	Chr14	54,870,335	54,870,335
nssv17220717	Remapped	Perfect	NC_000014.8:g.5533 7053_55337054ins27 9	GRCh37.p13	First Pass	NC_000014.8	Chr14	55,337,053	55,337,053

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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