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dbVar

Database of genomic structural variation

nsv5657458

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: 114 SVs from 24 studies. See in: genome view

Submitted genomic12,170,084-12,170,084

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5657458	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	12,170,084	12,170,084
nsv5657458	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	12,280,899	12,280,899

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17103135	insertion	SAMN00249890	Sequencing	Sequence alignment	1,169

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17103135	Submitted genomic		NC_000019.10:g.121 70084_12170085ins1 35	GRCh38 (hg38)		NC_000019.10	Chr19	12,170,084	12,170,084
nssv17103135	Remapped	Perfect	NC_000019.9:g.1228 0899_12280900ins13 5	GRCh37.p13	First Pass	NC_000019.9	Chr19	12,280,899	12,280,899

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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