A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989732



Internal ID12974810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:53137011..53189211hg38UCSC Ensembl
Innerchr2:53364149..53416349hg19UCSC Ensembl
Innerchr2:53217653..53269853hg18UCSC Ensembl
Innerchr2:53275800..53328000hg17UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3852201
hg1952201
hg1852201
hg1752201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751897
Supporting Variants
SamplesBEC_542
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989732
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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