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dbVar

Database of genomic structural variation

nsv5681003

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: 121 SVs from 25 studies. See in: genome view

Submitted genomic111,689,024-111,689,024

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5681003	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	111,689,024	111,689,024
nsv5681003	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	112,010,227	112,010,227

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17179601	alu insertion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17179601	Submitted genomic		NC_000006.12:g.111 689024_111689025in s280	GRCh38 (hg38)		NC_000006.12	Chr6	111,689,024	111,689,024
nssv17179601	Remapped	Perfect	NC_000006.11:g.112 010227_112010228in s280	GRCh37.p13	First Pass	NC_000006.11	Chr6	112,010,227	112,010,227

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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