A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593225



Internal ID16380634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:827702..870129hg38UCSC Ensembl
Innerchr4:821490..863917hg19UCSC Ensembl
Innerchr4:811490..853917hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3842428
hg1942428
hg1842428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8879n54
Supporting Variantsnssv1153429
SamplesHGDP00684
Known GenesGAK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593225
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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