A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577644



Internal ID16365053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73093559..73144157hg38UCSC Ensembl
Innerchr18:70760794..70811392hg19UCSC Ensembl
Innerchr18:68911774..68962372hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3850599
hg1950599
hg1850599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887372
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577644
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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