A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685040



Internal ID15421692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69023863..69024446hg38UCSC Ensembl
Innerchr15:69316203..69316786hg19UCSC Ensembl
Innerchr15:67103257..67103840hg18UCSC Ensembl
Innerchr15:67103257..67103840hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38584
hg19584
hg18584
hg17584
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521203
Supporting Variants
Samples
Known GenesMIR548H4, NOX5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685040
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