A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv168n21



Internal ID18990641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83605594..83610185hg38UCSC Ensembl
chr16:83639199..83643790hg19UCSC Ensembl
chr16:82196700..82201291hg18UCSC Ensembl
chr16:82196700..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 Variants
Supporting Variantsnsv521265, nsv521708
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv168n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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