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dbVar

Database of genomic structural variation

nsv5980355

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: 155 SVs from 28 studies. See in: genome view

Submitted genomic68,745,584-68,745,584

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5980355	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	68,745,584	68,745,584
nsv5980355	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	68,779,487	68,779,487

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17387540	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17387540	Submitted genomic		NC_000016.10:g.687 45584_68745585ins5 8	GRCh38 (hg38)		NC_000016.10	Chr16	68,745,584	68,745,584
nssv17387540	Remapped	Perfect	NC_000016.9:g.6877 9487_68779488ins58	GRCh37.p13	First Pass	NC_000016.9	Chr16	68,779,487	68,779,487

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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