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

dbVar

Database of genomic structural variation

nsv3565924

Organism: Homo sapiens

Study:nstd152 (Chaisson et al. 2019)
Variant Type:mobile element insertion
Method Type:Sequencing
Submitted on:GRCh38 (hg38)

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

Description:Insertion of a Alu mobile element relative to the reference
Publication(s):Chaisson et al. 2019

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

Submitted genomic91,318,180-91,318,210

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3565924	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	91,318,195 (-15, +15)	91,318,195 (-15, +15)
nsv3565924	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	94,080,477 (-15, +15)	94,080,477 (-15, +15)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
nssv14348857	alu insertion	SAMN00006466	Sequencing	Sequence alignment	Heterozygous	14,137

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14348857	Submitted genomic		NC_000009.12:g.(91 318180_91318210)_( 91318180_91318210) ins281	GRCh38 (hg38)		NC_000009.12	Chr9	91,318,195 (-15, +15)	91,318,195 (-15, +15)
nssv14348857	Remapped	Perfect	NC_000009.11:g.(94 080462_94080492)_( 94080462_94080492) ins281	GRCh37.p13	First Pass	NC_000009.11	Chr9	94,080,477 (-15, +15)	94,080,477 (-15, +15)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

You are here: NCBI