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dbVar

Database of genomic structural variation

nsv4766985

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37

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

Publication(s):Quan 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: 89 SVs from 23 studies. See in: genome view

Remapped(Score: Perfect):57,245,566-57,245,566

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4766985	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	57,245,566	57,245,566
nsv4766985	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	57,756,934	57,756,934

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16275031	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16275031	Remapped	Perfect	NC_000019.10:g.572 45566_57245567ins1 27	GRCh38.p12	First Pass	NC_000019.10	Chr19	57,245,566	57,245,566
nssv16275031	Submitted genomic		NC_000019.9:g.5775 6934_57756935ins12 7	GRCh37 (hg19)		NC_000019.9	Chr19	57,756,934	57,756,934

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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