A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515825



Internal ID15096432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83162159..83168288hg38UCSC Ensembl
Innerchr16:83195764..83201893hg19UCSC Ensembl
Innerchr16:81753265..81759394hg18UCSC Ensembl
Innerchr16:81753265..81759394hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg386130
hg196130
hg186130
hg176130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv680615, nssv671890, nssv688293, nssv683319, nssv685639, nssv665331, nssv674120, nssv672862, nssv689454, nssv665647, nssv682019, nssv684616, nssv664894, nssv663421
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515825
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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