A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2985n100



Internal ID22789072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55750518..55788045hg38UCSC Ensembl
chr16:55784430..55821957hg19UCSC Ensembl
chr16:54341931..54379458hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3837528
hg1937528
hg1837528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057284, nsv1058321, nsv1063302
Samples
Known GenesCES1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2985n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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