A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557759



Internal ID15998482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:23579455..23591232hg38UCSC Ensembl
Innerchr12:23732389..23744166hg19UCSC Ensembl
Innerchr12:23623656..23635433hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3811778
hg1911778
hg1811778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv789585, nssv789584
Samples
Known GenesSOX5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557759
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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