A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3019n100



Internal ID20154635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74834429..74955590hg38UCSC Ensembl
chr16:74868327..74989488hg19UCSC Ensembl
chr16:73425828..73546989hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38121162
hg19121162
hg18121162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059764, nsv1064546
Samples
Known GenesWDR59
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3019n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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