A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834845



Internal ID16128801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474226..105475033hg38UCSC Ensembl
Innerchr14:105940563..105941370hg19UCSC Ensembl
Innerchr14:105011608..105012415hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38808
hg19808
hg18808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566230
Supporting Variants
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834845
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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