A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982086



Internal ID12974421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97146572..97255390hg38UCSC Ensembl
Innerchr11:97017572..97126390hg19UCSC Ensembl
Innerchr11:96522782..96631600hg18UCSC Ensembl
Innerchr11:96522782..96631600hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38108819
hg19108819
hg18108819
hg17108819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751037
Supporting Variants
SamplesBEC_519
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982086
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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