A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152621



Internal ID15879289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7520075..7543152hg38UCSC Ensembl
Innerchr4:7521802..7544879hg19UCSC Ensembl
Innerchr4:7572702..7595779hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3823078
hg1923078
hg1823078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593614
Supporting Variants
SamplesHGDP01339
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152621
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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