A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577022



Internal ID16017745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:57047085..57074442hg38UCSC Ensembl
Innerchr18:54714316..54741673hg19UCSC Ensembl
Innerchr18:52865314..52892671hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3827358
hg1927358
hg1827358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5954n54
Supporting Variantsnssv1150599
SamplesHGDP01152
Known GenesLINC-ROR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577022
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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