A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv785880



Internal ID15733150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:753823..760447hg38UCSC Ensembl
Innerchr12:862989..869613hg19UCSC Ensembl
Innerchr12:733250..739874hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg386625
hg196625
hg186625
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556901
Supporting Variants
Samples
Known GenesWNK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv785880
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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