A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148712



Internal ID15533090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104660017..104723167hg38UCSC Ensembl
Innerchr14:105126354..105189504hg19UCSC Ensembl
Innerchr14:104197399..104260549hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3863151
hg1963151
hg1863151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566049
Supporting Variants
SamplesNINDS_105
Known GenesINF2, MIR4710
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148712
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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