A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614813



Internal ID16402222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88534209..88535071hg38UCSC Ensembl
Innerchr9:91149124..91149986hg19UCSC Ensembl
Innerchr9:90338944..90339806hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38863
hg19863
hg18863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12786n54
Supporting Variantsnssv1139162, nssv1139163, nssv1139166, nssv1139159, nssv1139161, nssv1139164, nssv1139167, nssv1139165, nssv1139158, nssv1139160, nssv1139169, nssv1139168
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614813
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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