A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548091



Internal ID15988814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:165634052..165634887hg38UCSC Ensembl
Innerchr1:165603289..165604124hg19UCSC Ensembl
Innerchr1:163869913..163870748hg18UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38836
hg19836
hg18836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv611n54
Supporting Variantsnssv727713
Samples
Known GenesMGST3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548091
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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