A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2529n100



Internal ID19012897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30608663..30796262hg38UCSC Ensembl
chr15:30900866..31088465hg19UCSC Ensembl
chr15:28688158..28875757hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38187600
hg19187600
hg18187600
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053960, nsv1041622, nsv1048016
Samples
Known GenesARHGAP11B, GOLGA8H, LOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2529n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss3
Observed Complex0
Frequencyn/a


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