A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv805442



Internal ID15752712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:131701606..131719949hg38UCSC Ensembl
Innerchr12:132186151..132204494hg19UCSC Ensembl
Innerchr12:130752104..130770447hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3818344
hg1918344
hg1818344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560926
Supporting Variants
Samples
Known GenesSFSWAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv805442
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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