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dbVar

Database of genomic structural variation

nsv5976471

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: 117 SVs from 32 studies. See in: genome view

Submitted genomic23,853,966-23,853,966

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5976471	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	23,853,966	23,853,966
nsv5976471	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	23,865,287	23,865,287

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17383980	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17383980	Submitted genomic		NC_000016.10:g.238 53966_23853967ins3 28	GRCh38 (hg38)		NC_000016.10	Chr16	23,853,966	23,853,966
nssv17383980	Remapped	Perfect	NC_000016.9:g.2386 5287_23865288ins32 8	GRCh37.p13	First Pass	NC_000016.9	Chr16	23,865,287	23,865,287

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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