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dbVar

Database of genomic structural variation

nsv5971229

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: 105 SVs from 22 studies. See in: genome view

Submitted genomic64,377,489-64,377,489

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5971229	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	64,377,489	64,377,489
nsv5971229	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	64,669,688	64,669,688

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17371831	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17371831	Submitted genomic		NC_000015.10:g.643 77489_64377490ins1 70	GRCh38 (hg38)		NC_000015.10	Chr15	64,377,489	64,377,489
nssv17371831	Remapped	Perfect	NC_000015.9:g.6466 9688_64669689ins17 0	GRCh37.p13	First Pass	NC_000015.9	Chr15	64,669,688	64,669,688

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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