A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577051



Internal ID16017774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59313335..59354317hg38UCSC Ensembl
Innerchr18:56980567..57021549hg19UCSC Ensembl
Innerchr18:55131547..55172529hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3840983
hg1940983
hg1840983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv884910
Samples
Known GenesCPLX4, LMAN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577051
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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