A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701455



Internal ID15438107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109012208..109024375hg38UCSC Ensembl
Innerchr13:109664556..109676723hg19UCSC Ensembl
Innerchr13:108462557..108474724hg18UCSC Ensembl
Innerchr13:108462557..108474724hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3812168
hg1912168
hg1812168
hg1712168
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525337
Supporting Variants
Samples
Known GenesMYO16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701455
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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