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dbVar

Database of genomic structural variation

nsv5962859

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: 136 SVs from 20 studies. See in: genome view

Submitted genomic168,559,733-168,559,733

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5962859	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	168,559,733	168,559,733
nsv5962859	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	169,416,243	169,416,243

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17401167	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17401167	Submitted genomic		NC_000002.12:g.168 559733_168559734in s165	GRCh38 (hg38)		NC_000002.12	Chr2	168,559,733	168,559,733
nssv17401167	Remapped	Perfect	NC_000002.11:g.169 416243_169416244in s165	GRCh37.p13	First Pass	NC_000002.11	Chr2	169,416,243	169,416,243

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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