A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515680



Internal ID15096287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83622659..83627861hg38UCSC Ensembl
Innerchr16:83656264..83661466hg19UCSC Ensembl
Innerchr16:82213765..82218967hg18UCSC Ensembl
Innerchr16:82213765..82218967hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg385203
hg195203
hg185203
hg175203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664366, nssv684502, nssv683378, nssv675669, nssv687428, nssv685979
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515680
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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