A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv993086



Internal ID16287042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15002272..15005183hg38UCSC Ensembl
Innerchr4:15003896..15006807hg19UCSC Ensembl
Innerchr4:14612994..14615905hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382912
hg192912
hg182912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593761
Supporting Variants
Samples
Known GenesCPEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv993086
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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