A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593872



Internal ID16034595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26843052..27076754hg38UCSC Ensembl
Innerchr4:26844674..27078376hg19UCSC Ensembl
Innerchr4:26453772..26687474hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38233703
hg19233703
hg18233703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152907
SamplesHGDP00376
Known GenesSTIM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593872
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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