A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548096



Internal ID16335505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:165634629..165635552hg38UCSC Ensembl
Innerchr1:165603866..165604789hg19UCSC Ensembl
Innerchr1:163870490..163871413hg18UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38924
hg19924
hg18924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv727723
Samples
Known GenesMGST3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548096
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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