A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577643



Internal ID16365052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73078389..73108504hg38UCSC Ensembl
Innerchr18:70745624..70775739hg19UCSC Ensembl
Innerchr18:68896604..68926719hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3830116
hg1930116
hg1830116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150629
Samples1782681080_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577643
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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