A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981903



Internal ID12974113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:54426430..54533322hg38UCSC Ensembl
Innerchr16:54460342..54567234hg19UCSC Ensembl
Innerchr16:53017843..53124735hg18UCSC Ensembl
Innerchr16:53017843..53124735hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38106893
hg19106893
hg18106893
hg17106893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751609
Supporting Variants
SamplesBEC_500
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981903
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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