A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983231



Internal ID12975032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25440265..25560165hg38UCSC Ensembl
Innerchr11:25461811..25581711hg19UCSC Ensembl
Innerchr11:25418387..25538287hg18UCSC Ensembl
Innerchr11:25418387..25538287hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38119901
hg19119901
hg18119901
hg17119901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751021
Supporting Variants
SamplesBEC_558
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983231
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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