A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559481



Internal ID16346890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:81736586..81750556hg38UCSC Ensembl
Innerchr12:82130365..82144335hg19UCSC Ensembl
Innerchr12:80654496..80668466hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3813971
hg1913971
hg1813971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2730n54
Supporting Variantsnssv798946, nssv798945, nssv798947
Samples
Known GenesPPFIA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559481
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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