A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982085



Internal ID12974420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97135302..97238243hg38UCSC Ensembl
Innerchr11:97006302..97109243hg19UCSC Ensembl
Innerchr11:96511512..96614453hg18UCSC Ensembl
Innerchr11:96511512..96614453hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38102942
hg19102942
hg18102942
hg17102942
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)essv6982085
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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