A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577082



Internal ID16364491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62039493..62040252hg38UCSC Ensembl
Innerchr18:59706726..59707485hg19UCSC Ensembl
Innerchr18:57857706..57858465hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38760
hg19760
hg18760
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5965n54
Supporting Variantsnssv884976, nssv884979, nssv884978, nssv884972, nssv884967, nssv884975, nssv884974, nssv884971, nssv884969, nssv884970, nssv884968, nssv884966, nssv884973, nssv884977
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577082
Frequency
Sample Size17421
Observed Gain12
Observed Loss2
Observed Complex0
Frequencyn/a


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