A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839482



Internal ID15786752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30620624..30672369hg38UCSC Ensembl
Innerchr15:30912827..30964572hg19UCSC Ensembl
Innerchr15:28700119..28751864hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3851746
hg1951746
hg1851746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568752
Supporting Variants
Samples
Known GenesARHGAP11B, LOC100288637
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839482
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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