A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3022n100



Internal ID22789109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75921526..76005861hg38UCSC Ensembl
chr16:75955424..76039759hg19UCSC Ensembl
chr16:74512925..74597260hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3884336
hg1984336
hg1884336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063509, nsv1056427
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3022n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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