A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3277n100



Internal ID22789364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68082268..68189163hg38UCSC Ensembl
chr17:66078392..66185304hg19UCSC Ensembl
chr17:63590029..63696899hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38106896
hg19106913
hg18106871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062505, nsv1065029, nsv1056977, nsv1060559
Samples
Known GenesLINC00674
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3277n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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