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dbVar

Database of genomic structural variation

nsv6250262

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: 88 SVs from 21 studies. See in: genome view

Submitted genomic50,097,317-50,097,317

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6250262	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	50,097,317	50,097,317
nsv6250262	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	50,131,228	50,131,228

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17847210	alu insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17847210	Submitted genomic		NC_000016.10:g.500 97317_50097318ins2 79	GRCh38 (hg38)		NC_000016.10	Chr16	50,097,317	50,097,317
nssv17847210	Remapped	Perfect	NC_000016.9:g.5013 1228_50131229ins27 9	GRCh37.p13	First Pass	NC_000016.9	Chr16	50,131,228	50,131,228

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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