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dbVar

Database of genomic structural variation

nsv5965927

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

Submitted genomic99,862,549-99,862,549

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5965927	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	99,862,549	99,862,549
nsv5965927	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	102,624,831	102,624,831

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17440763	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17440763	Submitted genomic		NC_000009.12:g.998 62549_99862550ins1 67	GRCh38 (hg38)		NC_000009.12	Chr9	99,862,549	99,862,549
nssv17440763	Remapped	Perfect	NC_000009.11:g.102 624831_102624832in s167	GRCh37.p13	First Pass	NC_000009.11	Chr9	102,624,831	102,624,831

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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