A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175452



Internal ID15527896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:27288899..27339805hg38UCSC Ensembl
Innerchr12:27441832..27492738hg19UCSC Ensembl
Innerchr12:27333099..27384005hg18UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg3850907
hg1950907
hg1850907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557808
Supporting Variants
SamplesHGDP00557
Known GenesARNTL2, STK38L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175452
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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