A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556915



Internal ID16344324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:757691..764367hg38UCSC Ensembl
Innerchr12:866857..873533hg19UCSC Ensembl
Innerchr12:737118..743794hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg386677
hg196677
hg186677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2259n54
Supporting Variantsnssv785923, nssv785921, nssv785935, nssv785940, nssv785937, nssv785933, nssv785936, nssv785941, nssv785944, nssv785930, nssv785946, nssv785947, nssv785942, nssv785927, nssv785949, nssv785945, nssv785925, nssv785931, nssv785920, nssv785929, nssv785928, nssv785938, nssv785926, nssv785934, nssv785924, nssv785922, nssv785939, nssv785948, nssv785943, nssv785932
Samples
Known GenesWNK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556915
Frequency
Sample Size17421
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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