A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521203



Internal ID15448496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69023863..69024446hg38UCSC Ensembl
Innerchr15:69316203..69316786hg19UCSC Ensembl
Innerchr15:67103257..67103840hg18UCSC Ensembl
Innerchr15:67103257..67103840hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38584
hg19584
hg18584
hg17584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv687957, nssv685040, nssv685092, nssv693097
Samples
Known GenesMIR548H4, NOX5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521203
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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