Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6261241

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: 122 SVs from 33 studies. See in: genome view

Submitted genomic31,066,606-31,066,606

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6261241	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	31,066,606	31,066,606
nsv6261241	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	31,106,222	31,106,222

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17859986	alu insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17859986	Submitted genomic		NC_000007.14:g.310 66606_31066607ins2 80	GRCh38 (hg38)		NC_000007.14	Chr7	31,066,606	31,066,606
nssv17859986	Remapped	Perfect	NC_000007.13:g.311 06222_31106223ins2 80	GRCh37.p13	First Pass	NC_000007.13	Chr7	31,106,222	31,106,222

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

You are here: NCBI