A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597309



Internal ID16384718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:16791748..16837753hg38UCSC Ensembl
Innerchr5:16791857..16837862hg19UCSC Ensembl
Innerchr5:16844857..16890862hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3846006
hg1946006
hg1846006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1026289
Samples
Known GenesMYO10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597309
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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