A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2523n100



Internal ID19012891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30373358..30654454hg38UCSC Ensembl
chr15:30665561..30946657hg19UCSC Ensembl
chr15:28452853..28733949hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38281097
hg19281097
hg18281097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037466, nsv1051353
Samples
Known GenesARHGAP11B, CHRFAM7A, GOLGA8H, LOC100288637, LOC101059918, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2523n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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