A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979349



Internal ID12980038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26294060..26365363hg38UCSC Ensembl
Innerchr14:26763266..26834569hg19UCSC Ensembl
Innerchr14:25833106..25904409hg18UCSC Ensembl
Innerchr14:25833106..25904409hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3871304
hg1971304
hg1871304
hg1771304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35052
Supporting Variants
SamplesNA18532
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979349
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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