A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677394



Internal ID15414046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:16673576..16679857hg38UCSC Ensembl
Innerchr5:16673685..16679966hg19UCSC Ensembl
Innerchr5:16726685..16732966hg18UCSC Ensembl
Innerchr5:16726685..16732966hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg386282
hg196282
hg186282
hg176282
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516145
Supporting Variants
Samples
Known GenesMYO10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677394
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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