A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522936



Internal ID15103543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83106638..83107072hg38UCSC Ensembl
Innerchr16:83140243..83140677hg19UCSC Ensembl
Innerchr16:81697744..81698178hg18UCSC Ensembl
Innerchr16:81697744..81698178hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38435
hg19435
hg18435
hg17435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698599
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522936
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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