A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983337



Internal ID12976135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:84417099..85223531hg38UCSC Ensembl
Innerchr14:84883443..85689875hg19UCSC Ensembl
Innerchr14:83953196..84759628hg18UCSC Ensembl
Innerchr14:83953196..84759628hg17UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg38806433
hg19806433
hg18806433
hg17806433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751288
Supporting Variants
SamplesBEC_64
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983337
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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