A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843972



Internal ID16137928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65354747..65356526hg38UCSC Ensembl
Innerchr15:65647085..65648864hg19UCSC Ensembl
Innerchr15:63434138..63435917hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381780
hg191780
hg181780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569707
Supporting Variants
Samples
Known GenesIGDCC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843972
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