A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556914



Internal ID15997637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:757691..763878hg38UCSC Ensembl
Innerchr12:866857..873044hg19UCSC Ensembl
Innerchr12:737118..743305hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg386188
hg196188
hg186188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2259n54
Supporting Variantsnssv785916, nssv785919, nssv785918, nssv785908, nssv785917, nssv785912, nssv785907, nssv785915, nssv785911, nssv785909, nssv785910, nssv785914, nssv785913
Samples
Known GenesWNK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556914
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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