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dbVar

Database of genomic structural variation

nsv5668735

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Ebert et al. 2021

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: 175 SVs from 33 studies. See in: genome view

Submitted genomic63,049,159-63,049,159

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5668735	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	63,049,159	63,049,159
nsv5668735	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	61,680,511	61,680,511

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17117445	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17117445	Submitted genomic		NC_000020.11:g.630 49159_63049160ins6 33	GRCh38 (hg38)		NC_000020.11	Chr20	63,049,159	63,049,159
nssv17117445	Remapped	Perfect	NC_000020.10:g.616 80511_61680512ins6 33	GRCh37.p13	First Pass	NC_000020.10	Chr20	61,680,511	61,680,511

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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