A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2736n100



Internal ID19013104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12723559..12787221hg38UCSC Ensembl
chr16:12817416..12881078hg19UCSC Ensembl
chr16:12724917..12788579hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3863663
hg1963663
hg1863663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036493, nsv1052892
Samples
Known GenesCPPED1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2736n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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