A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577255



Internal ID16017978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66316916..66722766hg38UCSC Ensembl
Innerchr18:63984153..64390003hg19UCSC Ensembl
Innerchr18:62135133..62540983hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38405851
hg19405851
hg18405851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv886014
Samples
Known GenesCDH19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577255
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer