A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045163



Internal ID19134382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55150155..55457310hg38UCSC Ensembl
Innerchr10:56909915..57217070hg19UCSC Ensembl
Innerchr10:56579921..56887076hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38307156
hg19307156
hg18307156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv865n100
Supporting Variantsnssv3507978
Samples
Known GenesRNU6-59P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045163
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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