A curated catalogue of human genomic structural variation




Variant Details

Variant: esv35052



Internal ID12991088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26294054..26365363hg38UCSC Ensembl
Innerchr14:26763260..26834569hg19UCSC Ensembl
Innerchr14:25833100..25904409hg18UCSC Ensembl
Innerchr14:25833100..25904409hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3871310
hg1971310
hg1871310
hg1771310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6979349, essv6979348
SamplesNA18532
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv35052
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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