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dbVar

Database of genomic structural variation

nsv5650316

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: 557 SVs from 47 studies. See in: genome view

Submitted genomic101,692,256-101,692,256

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5650316	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	101,692,256	101,692,256
nsv5650316	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	102,232,459	102,232,459

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17094486	insertion	SAMN00801888	Sequencing	Sequence alignment	2,004

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17094486	Submitted genomic		NC_000015.10:g.101 692256_101692257in s62	GRCh38 (hg38)		NC_000015.10	Chr15	101,692,256	101,692,256
nssv17094486	Remapped	Perfect	NC_000015.9:g.1022 32459_102232460ins 62	GRCh37.p13	First Pass	NC_000015.9	Chr15	102,232,459	102,232,459

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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