A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577792



Internal ID16365201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78904551..78916102hg38UCSC Ensembl
Innerchr18:76664551..76676102hg19UCSC Ensembl
Innerchr18:74765539..74777090hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3811552
hg1911552
hg1811552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv888830
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577792
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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