A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153600



Internal ID15877582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:145688438..145764212hg38UCSC Ensembl
Innerchr5:145068001..145143775hg19UCSC Ensembl
Innerchr5:145048194..145123968hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3875775
hg1975775
hg1875775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599934
Supporting Variants
SamplesHGDP01010
Known GenesPRELID2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153600
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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