A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569909



Internal ID16010632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71885318..71958400hg38UCSC Ensembl
Innerchr15:72177659..72250741hg19UCSC Ensembl
Innerchr15:69964713..70037795hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3873083
hg1973083
hg1873083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149598
SamplesNINDS_146
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569909
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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