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dbVar

Database of genomic structural variation

nsv5975413

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: 164 SVs from 30 studies. See in: genome view

Submitted genomic72,702,802-72,702,802

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5975413	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	72,702,802	72,702,802
nsv5975413	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	72,995,143	72,995,143

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17379745	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17379745	Submitted genomic		NC_000015.10:g.727 02802_72702803ins2 25	GRCh38 (hg38)		NC_000015.10	Chr15	72,702,802	72,702,802
nssv17379745	Remapped	Perfect	NC_000015.9:g.7299 5143_72995144ins22 5	GRCh37.p13	First Pass	NC_000015.9	Chr15	72,995,143	72,995,143

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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