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dbVar

Database of genomic structural variation

nsv5965635

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: 90 SVs from 24 studies. See in: genome view

Submitted genomic15,252,819-15,252,819

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5965635	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	15,252,819	15,252,819
nsv5965635	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	15,294,326	15,294,326

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17418524	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17418524	Submitted genomic		NC_000003.12:g.152 52819_15252820ins3 18	GRCh38 (hg38)		NC_000003.12	Chr3	15,252,819	15,252,819
nssv17418524	Remapped	Perfect	NC_000003.11:g.152 94326_15294327ins3 18	GRCh37.p13	First Pass	NC_000003.11	Chr3	15,294,326	15,294,326

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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