A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148965



Internal ID15876022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95632370..95658180hg38UCSC Ensembl
Innerchr14:96098707..96124517hg19UCSC Ensembl
Innerchr14:95168460..95194270hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3825811
hg1925811
hg1825811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565644
Supporting Variants
SamplesHGDP00774
Known GenesTCL6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148965
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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