A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577108



Internal ID16364517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:64447840..64603380hg38UCSC Ensembl
Innerchr18:62115075..62270615hg19UCSC Ensembl
Innerchr18:60266055..60421595hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38155541
hg19155541
hg18155541
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5970n54
Supporting Variantsnssv1150019, nssv885010, nssv885012, nssv885011, nssv885009
SamplesNINDS_256
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577108
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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