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dbVar

Database of genomic structural variation

nsv5973798

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: 635 SVs from 50 studies. See in: genome view

Submitted genomic30,013,603-30,013,603

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5973798	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	30,013,603	30,013,603
nsv5973798	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	30,024,924	30,024,924

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17370682	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17370682	Submitted genomic		NC_000016.10:g.300 13603_30013604ins1 89	GRCh38 (hg38)		NC_000016.10	Chr16	30,013,603	30,013,603
nssv17370682	Remapped	Perfect	NC_000016.9:g.3002 4924_30024925ins18 9	GRCh37.p13	First Pass	NC_000016.9	Chr16	30,024,924	30,024,924

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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