A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525671



Internal ID15106278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89915950..89932386hg38UCSC Ensembl
Innerchr16:89982358..89998794hg19UCSC Ensembl
Innerchr16:88509859..88526295hg18UCSC Ensembl
Innerchr16:88509859..88526295hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3816437
hg1916437
hg1816437
hg1716437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701828
Samples
Known GenesMC1R, TUBB3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525671
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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