A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987943



Internal ID12626533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:82622003..82725703hg38UCSC Ensembl
Innerchr14:83088347..83192047hg19UCSC Ensembl
Innerchr14:82158100..82261800hg18UCSC Ensembl
Innerchr14:82158100..82261800hg17UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38103701
hg19103701
hg18103701
hg17103701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751286
Supporting Variants
SamplesBEC_389
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987943
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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