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dbVar

Database of genomic structural variation

nsv5962278

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: 98 SVs from 24 studies. See in: genome view

Submitted genomic153,108,701-153,108,701

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5962278	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	153,108,701	153,108,701
nsv5962278	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	153,429,836	153,429,836

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17428895	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17428895	Submitted genomic		NC_000006.12:g.153 108701_153108702in s387	GRCh38 (hg38)		NC_000006.12	Chr6	153,108,701	153,108,701
nssv17428895	Remapped	Perfect	NC_000006.11:g.153 429836_153429837in s387	GRCh37.p13	First Pass	NC_000006.11	Chr6	153,429,836	153,429,836

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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