A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576461



Internal ID16363870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9913909..9914947hg38UCSC Ensembl
Innerchr18:9913906..9914944hg19UCSC Ensembl
Innerchr18:9903906..9904944hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381039
hg191039
hg181039
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5852n54
Supporting Variantsnssv878093, nssv878089, nssv878096, nssv878090, nssv878097, nssv878095, nssv878094, nssv878092, nssv878091, nssv878088
Samples
Known GenesVAPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576461
Frequency
Sample Size17421
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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