A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038685



Internal ID18781216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90793892..90923447hg38UCSC Ensembl
Innerchr9:93556174..93685729hg19UCSC Ensembl
Innerchr9:92595995..92725550hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38129556
hg19129556
hg18129556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759783
Samples
Known GenesSYK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038685
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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