A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6977961



Internal ID12631709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:46424485..46591447hg38UCSC Ensembl
Innerchr2:46651624..46818586hg19UCSC Ensembl
Innerchr2:46505128..46672090hg18UCSC Ensembl
Innerchr2:46563275..46730237hg17UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38166963
hg19166963
hg18166963
hg17166963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34937
Supporting Variants
SamplesNA10847
Known GenesATP6V1E2, LOC100506142, LOC101805491, PIGF, RHOQ, TMEM247
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6977961
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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