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dbVar

Database of genomic structural variation

nsv5967811

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Almarri et al. 2020

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: 133 SVs from 29 studies. See in: genome view

Submitted genomic86,056,134-86,056,134

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5967811	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	86,056,134	86,056,134
nsv5967811	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	85,767,176	85,767,176

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17363510	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17363510	Submitted genomic		NC_000011.10:g.860 56134_86056135ins1 67	GRCh38 (hg38)		NC_000011.10	Chr11	86,056,134	86,056,134
nssv17363510	Remapped	Perfect	NC_000011.9:g.8576 7176_85767177ins16 7	GRCh37.p13	First Pass	NC_000011.9	Chr11	85,767,176	85,767,176

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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