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dbVar

Database of genomic structural variation

nsv6251025

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: 158 SVs from 34 studies. See in: genome view

Submitted genomic36,663,941-36,663,941

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6251025	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	36,663,941	36,663,941
nsv6251025	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	37,154,843	37,154,843

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17849447	alu insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17849447	Submitted genomic		NC_000019.10:g.366 63941_36663942ins2 81	GRCh38 (hg38)		NC_000019.10	Chr19	36,663,941	36,663,941
nssv17849447	Remapped	Perfect	NC_000019.9:g.3715 4843_37154844ins28 1	GRCh37.p13	First Pass	NC_000019.9	Chr19	37,154,843	37,154,843

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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