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dbVar

Database of genomic structural variation

nsv5654086

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: 123 SVs from 26 studies. See in: genome view

Submitted genomic55,495,233-55,495,233

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5654086	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	55,495,233	55,495,233
nsv5654086	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	56,006,600	56,006,600

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17107030	insertion	SAMN01096687	Sequencing	Sequence alignment	1,334

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17107030	Submitted genomic		NC_000019.10:g.554 95233_55495234ins6 1	GRCh38 (hg38)		NC_000019.10	Chr19	55,495,233	55,495,233
nssv17107030	Remapped	Perfect	NC_000019.9:g.5600 6600_56006601ins61	GRCh37.p13	First Pass	NC_000019.9	Chr19	56,006,600	56,006,600

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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