A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551503



Internal ID15992226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71552620..71568064hg38UCSC Ensembl
Innerchr10:73312377..73327821hg19UCSC Ensembl
Innerchr10:72982383..72997827hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3815445
hg1915445
hg1815445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174251
SamplesHGDP00884
Known GenesCDH23
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551503
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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