A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153112



Internal ID15875614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:167848082..167897804hg38UCSC Ensembl
Innerchr5:167275087..167324809hg19UCSC Ensembl
Innerchr5:167207665..167257387hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3849723
hg1949723
hg1849723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600254
Supporting Variants
SamplesHGDP00708
Known GenesTENM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153112
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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