A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190116



Internal ID21328962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96004661..96004661hg38UCSC Ensembl
chr3:95723505..95723505hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944735
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190116
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer