A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2509n100



Internal ID20154125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30212863..30529543hg38UCSC Ensembl
chr15:30505066..30821746hg19UCSC Ensembl
chr15:28292358..28609038hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38316681
hg19316681
hg18316681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040271, nsv1043141, nsv1038791, nsv1041150, nsv1045467
Samples
Known GenesCHRFAM7A, DKFZP434L187, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2509n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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