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dbVar

Database of genomic structural variation

nsv6251026

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

Submitted genomic36,665,215-36,665,215

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6251026	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	36,665,215	36,665,215
nsv6251026	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	37,156,117	37,156,117

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17849448	alu insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17849448	Submitted genomic		NC_000019.10:g.366 65215_36665216ins2 81	GRCh38 (hg38)		NC_000019.10	Chr19	36,665,215	36,665,215
nssv17849448	Remapped	Perfect	NC_000019.9:g.3715 6117_37156118ins28 1	GRCh37.p13	First Pass	NC_000019.9	Chr19	37,156,117	37,156,117

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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