A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548090



Internal ID15988813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:165633287..165635754hg38UCSC Ensembl
Innerchr1:165602524..165604991hg19UCSC Ensembl
Innerchr1:163869148..163871615hg18UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg382468
hg192468
hg182468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv727712
Samples
Known GenesMGST3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548090
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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