A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614856



Internal ID16055579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90841532..90842247hg38UCSC Ensembl
Innerchr9:93603814..93604529hg19UCSC Ensembl
Innerchr9:92643635..92644350hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38716
hg19716
hg18716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139321
Samples
Known GenesSYK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614856
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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