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dbVar

Database of genomic structural variation

nsv5955427

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

Submitted genomic17,721,383-17,721,383

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5955427	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	17,721,383	17,721,383
nsv5955427	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	17,723,006	17,723,006

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17422352	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17422352	Submitted genomic		NC_000004.12:g.177 21383_17721384ins2 20	GRCh38 (hg38)		NC_000004.12	Chr4	17,721,383	17,721,383
nssv17422352	Remapped	Perfect	NC_000004.11:g.177 23006_17723007ins2 20	GRCh37.p13	First Pass	NC_000004.11	Chr4	17,723,006	17,723,006

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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