A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5784n54



Internal ID20139208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77049144..77101828hg38UCSC Ensembl
chr17:75045226..75097910hg19UCSC Ensembl
chr17:72556821..72609505hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3852685
hg1952685
hg1852685
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576073, nsv576072, nsv576071
Samples
Known GenesLINC00338, MIR6516, SCARNA16, SEC14L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5784n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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