A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987612



Internal ID12630447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:43092234..43242436hg38UCSC Ensembl
Innerchr13:43666370..43816572hg19UCSC Ensembl
Innerchr13:42564370..42714572hg18UCSC Ensembl
Innerchr13:42564370..42714572hg17UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38150203
hg19150203
hg18150203
hg17150203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751145
Supporting Variants
SamplesBEC_715
Known GenesDNAJC15, ENOX1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987612
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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