A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551501



Internal ID15992224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71396488..71398316hg38UCSC Ensembl
Innerchr10:73156245..73158073hg19UCSC Ensembl
Innerchr10:72826251..72828079hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381829
hg191829
hg181829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750262
Samples
Known GenesCDH23
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551501
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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