A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3274n100



Internal ID20154890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64618099..64978067hg38UCSC Ensembl
chr17:62614217..62974185hg19UCSC Ensembl
chr17:60044679..60404647hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38359969
hg19359969
hg18359969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057123, nsv1056492
Samples
Known GenesAMZ2P1, LOC146880, LRRC37A3, MIR4315-1, MIR4315-2, MIR6080, PLEKHM1P, SMURF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3274n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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