A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2522n100



Internal ID20154138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30338750..30515727hg38UCSC Ensembl
chr15:30630953..30807930hg19UCSC Ensembl
chr15:28418245..28595222hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38176978
hg19176978
hg18176978
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036200, nsv1039563, nsv1054320, nsv1049256
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2522n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss9
Observed Complex0
Frequencyn/a


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