A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597298



Internal ID16384707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:16179085..16179758hg38UCSC Ensembl
Innerchr5:16179194..16179867hg19UCSC Ensembl
Innerchr5:16232194..16232867hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38674
hg19674
hg18674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9619n54
Supporting Variantsnssv1026272, nssv1026271
Samples
Known GenesMARCH11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597298
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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