A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577081



Internal ID16364490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62039493..62040192hg38UCSC Ensembl
Innerchr18:59706726..59707425hg19UCSC Ensembl
Innerchr18:57857706..57858405hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38700
hg19700
hg18700
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5965n54
Supporting Variantsnssv884965, nssv884961, nssv884964, nssv884959, nssv884963, nssv884958, nssv884960, nssv884962
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577081
Frequency
Sample Size17421
Observed Gain6
Observed Loss2
Observed Complex0
Frequencyn/a


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