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dbVar

Database of genomic structural variation

nsv5978578

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

Submitted genomic18,689,904-18,689,904

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5978578	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	18,689,904	18,689,904
nsv5978578	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	18,670,548	18,670,548

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17409328	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17409328	Submitted genomic		NC_000020.11:g.186 89904_18689905ins1 76	GRCh38 (hg38)		NC_000020.11	Chr20	18,689,904	18,689,904
nssv17409328	Remapped	Perfect	NC_000020.10:g.186 70548_18670549ins1 76	GRCh37.p13	First Pass	NC_000020.10	Chr20	18,670,548	18,670,548

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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