A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548095



Internal ID15988818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:165634435..165635003hg38UCSC Ensembl
Innerchr1:165603672..165604240hg19UCSC Ensembl
Innerchr1:163870296..163870864hg18UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38569
hg19569
hg18569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv612n54
Supporting Variantsnssv727721, nssv727722
Samples
Known GenesMGST3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548095
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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