A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521708



Internal ID15102315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83605594..83610185hg38UCSC Ensembl
Innerchr16:83639199..83643790hg19UCSC Ensembl
Innerchr16:82196700..82201291hg18UCSC Ensembl
Innerchr16:82196700..82201291hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg384592
hg194592
hg184592
hg174592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv168n21
Supporting Variantsnssv698332
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521708
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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