A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577021



Internal ID16017744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:57046933..57079287hg38UCSC Ensembl
Innerchr18:54714164..54746518hg19UCSC Ensembl
Innerchr18:52865162..52897516hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3832355
hg1932355
hg1832355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5954n54
Supporting Variantsnssv883732
Samples
Known GenesLINC-ROR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577021
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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