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dbVar

Database of genomic structural variation

nsv5958088

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: 137 SVs from 35 studies. See in: genome view

Submitted genomic95,561,529-95,561,529

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5958088	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	95,561,529	95,561,529
nsv5958088	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	96,009,405	96,009,405

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17430215	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17430215	Submitted genomic		NC_000006.12:g.955 61529_95561530ins3 23	GRCh38 (hg38)		NC_000006.12	Chr6	95,561,529	95,561,529
nssv17430215	Remapped	Perfect	NC_000006.11:g.960 09405_96009406ins3 23	GRCh37.p13	First Pass	NC_000006.11	Chr6	96,009,405	96,009,405

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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