A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv833726



Internal ID16127682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101560397..101562940hg38UCSC Ensembl
Innerchr14:102026734..102029277hg19UCSC Ensembl
Innerchr14:101096487..101099030hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg382544
hg192544
hg182544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565882
Supporting Variants
Samples
Known GenesDIO3, MIR1247
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv833726
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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