A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577284



Internal ID16364693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66903284..67004349hg38UCSC Ensembl
Innerchr18:64570521..64671586hg19UCSC Ensembl
Innerchr18:62721501..62822566hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38101066
hg19101066
hg18101066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6004n54
Supporting Variantsnssv886250
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577284
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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