A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482914



Internal ID15582282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33450161..33601719hg38UCSC Ensembl
Innerchr15:33742362..33893920hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38151559
hg19151559
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996092, nssv2995964
Samples
Known GenesRYR3
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv482914
Frequency
Sample Size39
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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