A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577692



Internal ID16365101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76699639..76757838hg38UCSC Ensembl
Innerchr18:74411595..74469794hg19UCSC Ensembl
Innerchr18:72540583..72598782hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3858200
hg1958200
hg1858200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6077n54
Supporting Variantsnssv887540
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577692
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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