A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517665



Internal ID15098272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82669950..82670086hg38UCSC Ensembl
Innerchr16:82703555..82703691hg19UCSC Ensembl
Innerchr16:81261056..81261192hg18UCSC Ensembl
Innerchr16:81261056..81261192hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38137
hg19137
hg18137
hg17137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675668, nssv663395, nssv677237, nssv667747, nssv686180, nssv688765, nssv688881, nssv663240, nssv666049, nssv660381, nssv676177, nssv664979, nssv652766, nssv671933, nssv690445, nssv666076, nssv681160, nssv688046
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517665
Frequency
Sample Size2026
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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