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dbVar

Database of genomic structural variation

nsv5961223

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: 139 SVs from 22 studies. See in: genome view

Submitted genomic168,520,596-168,520,596

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5961223	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	168,520,596	168,520,596
nsv5961223	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	169,377,106	169,377,106

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17392606	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17392606	Submitted genomic		NC_000002.12:g.168 520596_168520597in s109	GRCh38 (hg38)		NC_000002.12	Chr2	168,520,596	168,520,596
nssv17392606	Remapped	Perfect	NC_000002.11:g.169 377106_169377107in s109	GRCh37.p13	First Pass	NC_000002.11	Chr2	169,377,106	169,377,106

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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