A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751037



Internal ID12984589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97135302..97255390hg38UCSC Ensembl
Innerchr11:97006302..97126390hg19UCSC Ensembl
Innerchr11:96511512..96631600hg18UCSC Ensembl
Innerchr11:96511512..96631600hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38120089
hg19120089
hg18120089
hg17120089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6982085, essv6982087, essv6982086, essv6989568, essv6989569
SamplesBEC_519
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)esv2751037
Frequency
Sample Size771
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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