A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614855



Internal ID16055578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90841357..90842692hg38UCSC Ensembl
Innerchr9:93603639..93604974hg19UCSC Ensembl
Innerchr9:92643460..92644795hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg381336
hg191336
hg181336
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139320
Samples
Known GenesSYK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614855
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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