A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987901



Internal ID12972733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40592437..40741454hg38UCSC Ensembl
Innerchr11:40613987..40763004hg19UCSC Ensembl
Innerchr11:40570563..40719580hg18UCSC Ensembl
Innerchr11:40570563..40719580hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38149018
hg19149018
hg18149018
hg17149018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751023
Supporting Variants
SamplesBEC_345
Known GenesLRRC4C
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987901
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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