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dbVar

Database of genomic structural variation

nsv5965829

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: 131 SVs from 31 studies. See in: genome view

Submitted genomic74,520,191-74,520,191

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5965829	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	74,520,191	74,520,191
nsv5965829	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	74,569,342	74,569,342

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17424709	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17424709	Submitted genomic		NC_000003.12:g.745 20191_74520192ins2 18	GRCh38 (hg38)		NC_000003.12	Chr3	74,520,191	74,520,191
nssv17424709	Remapped	Perfect	NC_000003.11:g.745 69342_74569343ins2 18	GRCh37.p13	First Pass	NC_000003.11	Chr3	74,569,342	74,569,342

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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