A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4609n54



Internal ID20138033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71911176..72033254hg38UCSC Ensembl
chr15:72203517..72325595hg19UCSC Ensembl
chr15:69990571..70112649hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38122079
hg19122079
hg18122079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569910, nsv569912, nsv569911
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4609n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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