A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832726



Internal ID15779996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95656071..95670457hg38UCSC Ensembl
Innerchr14:96122408..96136794hg19UCSC Ensembl
Innerchr14:95192161..95206547hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3814387
hg1914387
hg1814387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565645
Supporting Variants
Samples
Known GenesTCL6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832726
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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