A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152673



Internal ID15529704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9832483..9862074hg38UCSC Ensembl
Innerchr4:9834107..9863698hg19UCSC Ensembl
Innerchr4:9443205..9472796hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3829592
hg1929592
hg1829592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593690
Supporting Variants
SamplesHGDP00832
Known GenesSLC2A9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152673
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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