A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986582



Internal ID12981713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:731469..823705hg38UCSC Ensembl
Innerchr5:731584..823820hg19UCSC Ensembl
Innerchr5:784584..876820hg18UCSC Ensembl
Innerchr5:784584..876820hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3892237
hg1992237
hg1892237
hg1792237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34972
Supporting Variants
SamplesNA18995
Known GenesZDHHC11
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986582
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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