A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520527



Internal ID15101134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74816295..74830515hg38UCSC Ensembl
Innerchr15:75108636..75122856hg19UCSC Ensembl
Innerchr15:72895689..72909909hg18UCSC Ensembl
Innerchr15:72895689..72909909hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3814221
hg1914221
hg1814221
hg1714221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689173, nssv672106
Samples
Known GenesCPLX3, LMAN1L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520527
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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