A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981902



Internal ID12974115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:54422713..54530061hg38UCSC Ensembl
Innerchr16:54456625..54563973hg19UCSC Ensembl
Innerchr16:53014126..53121474hg18UCSC Ensembl
Innerchr16:53014126..53121474hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38107349
hg19107349
hg18107349
hg17107349
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981902
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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