A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005884



Internal ID22067515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71511279..71521981hg38UCSC Ensembl
Outerchr10:71509935..71525606hg38UCSC Ensembl
Innerchr10:73271036..73281738hg19UCSC Ensembl
Outerchr10:73269692..73285363hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3815672
hg1915672
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154621
Supporting Variants
Samples
Known GenesCDH23
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005884
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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