A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556899



Internal ID15997622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:741447..813242hg38UCSC Ensembl
Innerchr12:850613..922408hg19UCSC Ensembl
Innerchr12:720874..792669hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3871796
hg1971796
hg1871796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176241
SamplesHGDP00206
Known GenesWNK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556899
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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