A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552555



Internal ID16339964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111200..133116440hg38UCSC Ensembl
Innerchr10:134924704..134929944hg19UCSC Ensembl
Innerchr10:134774694..134779934hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385241
hg195241
hg185241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv762093
Samples
Known GenesGPR123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552555
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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