A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv888562



Internal ID16182518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78013168..78140770hg38UCSC Ensembl
Innerchr18:75773172..75900770hg19UCSC Ensembl
Innerchr18:73874160..74001758hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38127603
hg19127599
hg18127599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577735
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv888562
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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