A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577549



Internal ID16364958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70284647..70287652hg38UCSC Ensembl
Innerchr18:67951883..67954888hg19UCSC Ensembl
Innerchr18:66102863..66105868hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg383006
hg193006
hg183006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6056n54
Supporting Variantsnssv887094, nssv887093
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577549
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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