A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2472n100



Internal ID22788559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24824408..24840511hg38UCSC Ensembl
chr15:25069555..25085658hg19UCSC Ensembl
chr15:22620648..22636751hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3816104
hg1916104
hg1816104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047530, nsv1035840, nsv1045030
Samples
Known GenesSNRPN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2472n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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