A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989773



Internal ID12976122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:84349003..85237703hg38UCSC Ensembl
Innerchr14:84815347..85704047hg19UCSC Ensembl
Innerchr14:83885100..84773800hg18UCSC Ensembl
Innerchr14:83885100..84773800hg17UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg38888701
hg19888701
hg18888701
hg17888701
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989773
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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