A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576779



Internal ID16364188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:44213865..44575808hg38UCSC Ensembl
Innerchr18:41793830..42155773hg19UCSC Ensembl
Innerchr18:40047828..40409771hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38361944
hg19361944
hg18361944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv882522
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576779
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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