A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152627



Internal ID15526170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8371217..8456667hg38UCSC Ensembl
Innerchr4:8372944..8458394hg19UCSC Ensembl
Innerchr4:8423844..8509294hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3885451
hg1985451
hg1885451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593638
Supporting Variants
SamplesHGDP00058
Known GenesACOX3, TRMT44
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152627
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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