A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548576



Internal ID16335985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:190994730..191380484hg38UCSC Ensembl
Innerchr1:190963860..191349614hg19UCSC Ensembl
Innerchr1:189230483..189616237hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38385755
hg19385755
hg18385755
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv732590
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548576
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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