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dbVar

Database of genomic structural variation

nsv5672497

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: 197 SVs from 36 studies. See in: genome view

Submitted genomic64,232,966-64,232,966

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5672497	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	64,232,966	64,232,966
nsv5672497	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	62,864,319	62,864,319

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17119222	insertion	SAMN00007824	Sequencing	Sequence alignment	1,699

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17119222	Submitted genomic		NC_000020.11:g.642 32966_64232967ins7 10	GRCh38 (hg38)		NC_000020.11	Chr20	64,232,966	64,232,966
nssv17119222	Remapped	Perfect	NC_000020.10:g.628 64319_62864320ins7 10	GRCh37.p13	First Pass	NC_000020.10	Chr20	62,864,319	62,864,319

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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