A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614814



Internal ID16402223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88534209..88537577hg38UCSC Ensembl
Innerchr9:91149124..91152492hg19UCSC Ensembl
Innerchr9:90338944..90342312hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg383369
hg193369
hg183369
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139170, nssv1139171
Samples
Known GenesNXNL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614814
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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