A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614812



Internal ID16402221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88534158..88539211hg38UCSC Ensembl
Innerchr9:91149073..91154126hg19UCSC Ensembl
Innerchr9:90338893..90343946hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg385054
hg195054
hg185054
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139157
Samples
Known GenesNXNL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614812
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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