A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv786698



Internal ID16080654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:2795206..2796171hg38UCSC Ensembl
Innerchr12:2904372..2905337hg19UCSC Ensembl
Innerchr12:2774633..2775598hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38966
hg19966
hg18966
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557081
Supporting Variants
Samples
Known GenesFKBP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv786698
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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