A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2750981



Internal ID12984533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:115612450..115870866hg38UCSC Ensembl
Innerchr11:115483168..115741584hg19UCSC Ensembl
Innerchr11:114988378..115246794hg18UCSC Ensembl
Innerchr11:114988378..115246794hg17UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38258417
hg19258417
hg18258417
hg17258417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6983326, essv6983325, essv6983327, essv6988656
SamplesBEC_639
Known GenesLINC00900
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)esv2750981
Frequency
Sample Size771
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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