A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148959



Internal ID15529841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76995358..77026548hg38UCSC Ensembl
Innerchr14:77461701..77492891hg19UCSC Ensembl
Innerchr14:76531454..76562644hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3831191
hg1931191
hg1831191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565210
Supporting Variants
SamplesHGDP00857
Known GenesIRF2BPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148959
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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