A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3294n100



Internal ID20154910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81415451..81473664hg38UCSC Ensembl
chr17:79389251..79440690hg19UCSC Ensembl
chr17:77003846..77055285hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3858214
hg1951440
hg1851440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058027, nsv1063998, nsv1058786, nsv1061268
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)dgv3294n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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