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dbVar

Database of genomic structural variation

nsv5965621

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: 103 SVs from 28 studies. See in: genome view

Submitted genomic45,133,739-45,133,739

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5965621	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	45,133,739	45,133,739
nsv5965621	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	45,175,231	45,175,231

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17411539	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17411539	Submitted genomic		NC_000003.12:g.451 33739_45133740ins2 09	GRCh38 (hg38)		NC_000003.12	Chr3	45,133,739	45,133,739
nssv17411539	Remapped	Perfect	NC_000003.11:g.451 75231_45175232ins2 09	GRCh37.p13	First Pass	NC_000003.11	Chr3	45,175,231	45,175,231

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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