A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2520n100



Internal ID19012888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30333873..30638297hg38UCSC Ensembl
chr15:30626076..30930500hg19UCSC Ensembl
chr15:28413368..28717792hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38304425
hg19304425
hg18304425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047893, nsv1037817, nsv1047413, nsv1040144, nsv1049758, nsv1054334, nsv1035513, nsv1036029, nsv1047174, nsv1051650
Samples
Known GenesARHGAP11B, CHRFAM7A, GOLGA8H, 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)dgv2520n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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