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dbVar

Database of genomic structural variation

nsv5968278

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Almarri et al. 2020

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: 238 SVs from 37 studies. See in: genome view

Submitted genomic14,090,084-14,090,084

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5968278	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	14,090,084	14,090,084
nsv5968278	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	14,200,896	14,200,896

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17394422	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17394422	Submitted genomic		NC_000019.10:g.140 90084_14090085ins1 58	GRCh38 (hg38)		NC_000019.10	Chr19	14,090,084	14,090,084
nssv17394422	Remapped	Perfect	NC_000019.9:g.1420 0896_14200897ins15 8	GRCh37.p13	First Pass	NC_000019.9	Chr19	14,200,896	14,200,896

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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