A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3295n100



Internal ID20154911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81415451..81485298hg38UCSC Ensembl
chr17:79389251..79452324hg19UCSC Ensembl
chr17:77003846..77066919hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3869848
hg1963074
hg1863074
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061314, nsv1058737, nsv1065757, nsv1062256
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)dgv3295n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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