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dbVar

Database of genomic structural variation

nsv5967195

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: 88 SVs from 18 studies. See in: genome view

Submitted genomic156,653,493-156,653,493

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5967195	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	156,653,493	156,653,493
nsv5967195	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	156,080,504	156,080,504

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17410483	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17410483	Submitted genomic		NC_000005.10:g.156 653493_156653494in s173	GRCh38 (hg38)		NC_000005.10	Chr5	156,653,493	156,653,493
nssv17410483	Remapped	Perfect	NC_000005.9:g.1560 80504_156080505ins 173	GRCh37.p13	First Pass	NC_000005.9	Chr5	156,080,504	156,080,504

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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