A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3030n100



Internal ID22789117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77638145..77709861hg38UCSC Ensembl
chr16:77672042..77743758hg19UCSC Ensembl
chr16:76229543..76301259hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3871717
hg1971717
hg1871717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059503, nsv1060619
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)dgv3030n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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