A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149233



Internal ID15853675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65272257..65333881hg38UCSC Ensembl
Innerchr15:65564595..65626219hg19UCSC Ensembl
Innerchr15:63351648..63413272hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3861625
hg1961625
hg1861625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569705
Supporting Variants
Samples1780854339_A
Known GenesIGDCC3, PARP16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149233
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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