A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552541



Internal ID16339950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133107631..133186655hg38UCSC Ensembl
Innerchr10:134921135..135000159hg19UCSC Ensembl
Innerchr10:134771125..134850149hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3879025
hg1979025
hg1879025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1465n54
Supporting Variantsnssv761982
Samples
Known GenesGPR123, KNDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552541
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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