A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593614



Internal ID16381023
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 StatusM
Merged Variantsdgv8954n54
Supporting Variantsnssv1152621
SamplesHGDP01339
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593614
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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