A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569910



Internal ID16010633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71911176..72003987hg38UCSC Ensembl
Innerchr15:72203517..72296328hg19UCSC Ensembl
Innerchr15:69990571..70083382hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3892812
hg1992812
hg1892812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4609n54
Supporting Variantsnssv844953
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569910
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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