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dbVar

Database of genomic structural variation

nsv6251094

Organism: Homo sapiens

Study:nstd215 (Prakrithi et al. 2022)
Variant Type:mobile element insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Prakrithi et al. 2022

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: 65 SVs from 20 studies. See in: genome view

Submitted genomic49,307,724-49,307,724

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6251094	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	49,307,724	49,307,724
nsv6251094	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	49,810,981	49,810,981

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17849928	alu insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17849928	Submitted genomic		NC_000019.10:g.493 07724_49307725ins2 67	GRCh38 (hg38)		NC_000019.10	Chr19	49,307,724	49,307,724
nssv17849928	Remapped	Perfect	NC_000019.9:g.4981 0981_49810982ins26 7	GRCh37.p13	First Pass	NC_000019.9	Chr19	49,810,981	49,810,981

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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