A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4611n54



Internal ID20138035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71969044..72033254hg38UCSC Ensembl
chr15:72261385..72325595hg19UCSC Ensembl
chr15:70048439..70112649hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3864211
hg1964211
hg1864211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569916, nsv569914
SamplesNINDS_223
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4611n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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