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dbVar

Database of genomic structural variation

nsv5972362

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: 125 SVs from 22 studies. See in: genome view

Submitted genomic67,785,731-67,785,731

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5972362	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	67,785,731	67,785,731
nsv5972362	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	67,819,634	67,819,634

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17372785	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17372785	Submitted genomic		NC_000016.10:g.677 85731_67785732ins2 64	GRCh38 (hg38)		NC_000016.10	Chr16	67,785,731	67,785,731
nssv17372785	Remapped	Perfect	NC_000016.9:g.6781 9634_67819635ins26 4	GRCh37.p13	First Pass	NC_000016.9	Chr16	67,819,634	67,819,634

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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