A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887389



Internal ID16181345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76386003..76395964hg38UCSC Ensembl
Innerchr18:74097959..74107920hg19UCSC Ensembl
Innerchr18:72226947..72236908hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg389962
hg199962
hg189962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577664
Supporting Variants
Samples
Known GenesZNF516
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv887389
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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