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dbVar

Database of genomic structural variation

nsv5952414

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 26 studies. See in: genome view

Submitted genomic105,533,416-105,533,416

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5952414	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	105,533,416	105,533,416
nsv5952414	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	108,295,697	108,295,697

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17431977	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17431977	Submitted genomic		NC_000009.12:g.105 533416_105533417in s160	GRCh38 (hg38)		NC_000009.12	Chr9	105,533,416	105,533,416
nssv17431977	Remapped	Perfect	NC_000009.11:g.108 295697_108295698in s160	GRCh37.p13	First Pass	NC_000009.11	Chr9	108,295,697	108,295,697

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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