A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752276



Internal ID12985828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11224627..11958106hg38UCSC Ensembl
Innerchr9:11224627..11958106hg19UCSC Ensembl
Innerchr9:11214627..11948106hg18UCSC Ensembl
Innerchr9:11214627..11948106hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38733480
hg19733480
hg18733480
hg17733480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6980663, essv6980664, essv6987830, essv6980662
SamplesBEC_101
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)esv2752276
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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