A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829090



Internal ID16123046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70928887..71158395hg38UCSC Ensembl
Innerchr14:71395604..71625112hg19UCSC Ensembl
Innerchr14:70465357..70694865hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38229509
hg19229509
hg18229509
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565043
Supporting Variants
Samples
Known GenesPCNX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv829090
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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