A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569603



Internal ID16010326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59317554..59389015hg38UCSC Ensembl
Innerchr15:59609753..59681214hg19UCSC Ensembl
Innerchr15:57397045..57468506hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3871462
hg1971462
hg1871462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149225
SamplesHGDP01179
Known GenesMYO1E
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569603
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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