A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980097



Internal ID12634562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130263320..130340106hg38UCSC Ensembl
Innerchr11:130133215..130210001hg19UCSC Ensembl
Innerchr11:129638425..129715211hg18UCSC Ensembl
Innerchr11:129638425..129715211hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3876787
hg1976787
hg1876787
hg1776787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34550
Supporting Variants
SamplesNA18952
Known GenesZBTB44
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980097
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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