A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051882



Internal ID18794413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121995657..122018988hg38UCSC Ensembl
Innerchr10:123755172..123778503hg19UCSC Ensembl
Innerchr10:123745162..123768493hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3823332
hg1923332
hg1823332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521844
Samples
Known GenesTACC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051882
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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