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dbVar

Database of genomic structural variation

nsv5672455

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: 131 SVs from 27 studies. See in: genome view

Submitted genomic36,396,348-36,396,348

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5672455	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	36,396,348	36,396,348
nsv5672455	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	35,024,751	35,024,751

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17116881	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
nssv17116881	Submitted genomic		NC_000020.11:g.363 96348_36396349ins1 466	GRCh38 (hg38)		NC_000020.11	Chr20	36,396,348	36,396,348
nssv17116881	Remapped	Perfect	NC_000020.10:g.350 24751_35024752ins1 466	GRCh37.p13	First Pass	NC_000020.10	Chr20	35,024,751	35,024,751

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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