A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523361



Internal ID15450654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33595566..33598341hg38UCSC Ensembl
Innerchr15:33887767..33890542hg19UCSC Ensembl
Innerchr15:31675059..31677834hg18UCSC Ensembl
Innerchr15:31675059..31677834hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382776
hg192776
hg182776
hg172776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699110
Samples
Known GenesRYR3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523361
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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