A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552546



Internal ID16339955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111147..133111936hg38UCSC Ensembl
Innerchr10:134924651..134925440hg19UCSC Ensembl
Innerchr10:134774641..134775430hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38790
hg19790
hg18790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1467n54
Supporting Variantsnssv761991
Samples
Known GenesGPR123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552546
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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