A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983674



Internal ID12629071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8425647..8649997hg38UCSC Ensembl
Innerchr11:8447194..8671544hg19UCSC Ensembl
Innerchr11:8403770..8628120hg18UCSC Ensembl
Innerchr11:8403770..8628120hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38224351
hg19224351
hg18224351
hg17224351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751035
Supporting Variants
SamplesBEC_611
Known GenesSTK33, TRIM66
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983674
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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