A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569929



Internal ID16010652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72094008..72110660hg38UCSC Ensembl
Innerchr15:72386349..72403001hg19UCSC Ensembl
Innerchr15:70173403..70190055hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3816653
hg1916653
hg1816653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845047
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569929
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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