A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577769



Internal ID16365178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78831635..78841203hg38UCSC Ensembl
Innerchr18:76591635..76601203hg19UCSC Ensembl
Innerchr18:74692623..74702191hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg389569
hg199569
hg189569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv888730
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577769
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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