A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527342



Internal ID15107949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83083756..83101084hg38UCSC Ensembl
Innerchr16:83117361..83134689hg19UCSC Ensembl
Innerchr16:81674862..81692190hg18UCSC Ensembl
Innerchr16:81674862..81692190hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3817329
hg1917329
hg1817329
hg1717329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703768
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527342
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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