A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34240



Internal ID12990279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22628701..22695594hg38UCSC Ensembl
Innerchr9:22628700..22695593hg19UCSC Ensembl
Innerchr9:22618700..22685593hg18UCSC Ensembl
Innerchr9:22618700..22685593hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3866894
hg1966894
hg1866894
hg1766894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6988160, essv6979359
SamplesNA18532
Known GenesFLJ35282
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)esv34240
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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