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dbVar

Database of genomic structural variation

nsv5977447

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: 173 SVs from 33 studies. See in: genome view

Submitted genomic16,216,786-16,216,786

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5977447	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	16,216,786	16,216,786
nsv5977447	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	16,120,100	16,120,100

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17372676	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17372676	Submitted genomic		NC_000017.11:g.162 16786_16216787ins1 80	GRCh38 (hg38)		NC_000017.11	Chr17	16,216,786	16,216,786
nssv17372676	Remapped	Perfect	NC_000017.10:g.161 20100_16120101ins1 80	GRCh37.p13	First Pass	NC_000017.10	Chr17	16,120,100	16,120,100

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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