A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520128



Internal ID15447421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:16737404..16746675hg38UCSC Ensembl
Innerchr5:16737513..16746784hg19UCSC Ensembl
Innerchr5:16790513..16799784hg18UCSC Ensembl
Innerchr5:16790513..16799784hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg389272
hg199272
hg189272
hg179272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661052, nssv687119
Samples
Known GenesMYO10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520128
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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