A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752288



Internal ID12985840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17965725..18036894hg38UCSC Ensembl
Innerchr9:17965723..18036892hg19UCSC Ensembl
Innerchr9:17955723..18026892hg18UCSC Ensembl
Innerchr9:17955723..18026892hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3871170
hg1971170
hg1871170
hg1771170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6982067, essv6982066
SamplesBEC_516
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752288
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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