A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593767



Internal ID16381176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15002656..15005133hg38UCSC Ensembl
Innerchr4:15004280..15006757hg19UCSC Ensembl
Innerchr4:14613378..14615855hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382478
hg192478
hg182478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8978n54
Supporting Variantsnssv993095
Samples
Known GenesCPEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593767
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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