A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3293n100



Internal ID20154909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81415451..81462332hg38UCSC Ensembl
chr17:79389251..79429358hg19UCSC Ensembl
chr17:77003846..77043953hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3846882
hg1940108
hg1840108
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056240, nsv1065921
Samples
Known GenesBAHCC1, MIR3186
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3293n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss3
Observed Complex0
Frequencyn/a


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