A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551502



Internal ID15992225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71402480..71687524hg38UCSC Ensembl
Innerchr10:73162237..73447281hg19UCSC Ensembl
Innerchr10:72832243..73117287hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38285045
hg19285045
hg18285045
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750263
Samples
Known GenesCDH23, MIR6797
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551502
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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