A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577546



Internal ID16364955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70075210..70204275hg38UCSC Ensembl
Innerchr18:67742446..67871511hg19UCSC Ensembl
Innerchr18:65893426..66022491hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38129066
hg19129066
hg18129066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887088
Samples
Known GenesRTTN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577546
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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