A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576660



Internal ID16364069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37641667..37753370hg38UCSC Ensembl
Innerchr18:35221630..35333334hg19UCSC Ensembl
Innerchr18:33475628..33587332hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38111704
hg19111705
hg18111705
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878967
Samples
Known GenesMIR4318
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576660
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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