A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982259



Internal ID12626774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12735149..12777782hg38UCSC Ensembl
Innerchr16:12829006..12871639hg19UCSC Ensembl
Innerchr16:12736507..12779140hg18UCSC Ensembl
Innerchr16:12736507..12779140hg17UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3842634
hg1942634
hg1842634
hg1742634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751549
Supporting Variants
SamplesBEC_408
Known GenesCPPED1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982259
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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