A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv805586



Internal ID15752856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132304240..132314294hg38UCSC Ensembl
Innerchr12:132880826..132890880hg19UCSC Ensembl
Innerchr12:131390899..131400953hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3810055
hg1910055
hg1810055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560993
Supporting Variants
Samples
Known GenesGALNT9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv805586
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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