A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577651



Internal ID16365060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74397012..74411029hg38UCSC Ensembl
Innerchr18:72064247..72078264hg19UCSC Ensembl
Innerchr18:70215227..70229244hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3814018
hg1914018
hg1814018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887377
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577651
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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