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dbVar

Database of genomic structural variation

nsv5952984

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: 192 SVs from 29 studies. See in: genome view

Submitted genomic42,880,945-42,880,945

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5952984	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	42,880,945	42,880,945
nsv5952984	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	42,736,088	42,736,088

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17441669	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17441669	Submitted genomic		NC_000008.11:g.428 80945_42880946ins4 02	GRCh38 (hg38)		NC_000008.11	Chr8	42,880,945	42,880,945
nssv17441669	Remapped	Perfect	NC_000008.10:g.427 36088_42736089ins4 02	GRCh37.p13	First Pass	NC_000008.10	Chr8	42,736,088	42,736,088

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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