A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551506



Internal ID15992229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71646197..71652980hg38UCSC Ensembl
Innerchr10:73405954..73412737hg19UCSC Ensembl
Innerchr10:73075960..73082743hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg386784
hg196784
hg186784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750264
Samples
Known GenesCDH23, MIR6797
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551506
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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