A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686675



Internal ID15423327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24109283..24240013hg38UCSC Ensembl
Innerchr15:24354430..24485160hg19UCSC Ensembl
Innerchr15:21905523..22036253hg18UCSC Ensembl
Innerchr15:21905523..22036253hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38130731
hg19130731
hg18130731
hg17130731
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517191
Supporting Variants
Samples
Known GenesPWRN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686675
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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