A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577693



Internal ID16365102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76699639..76759861hg38UCSC Ensembl
Innerchr18:74411595..74471817hg19UCSC Ensembl
Innerchr18:72540583..72600805hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3860223
hg1960223
hg1860223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6077n54
Supporting Variantsnssv887542, nssv887541
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577693
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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