A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989522



Internal ID12627278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:68861851..69012842hg38UCSC Ensembl
Innerchr16:68895754..69046745hg19UCSC Ensembl
Innerchr16:67453255..67604246hg18UCSC Ensembl
Innerchr16:67453255..67604246hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38150992
hg19150992
hg18150992
hg17150992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751611
Supporting Variants
SamplesBEC_48
Known GenesTANGO6
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989522
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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