A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053252



Internal ID18795783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90847850..90936821hg38UCSC Ensembl
Innerchr9:93610132..93699103hg19UCSC Ensembl
Innerchr9:92649953..92738924hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3888972
hg1988972
hg1888972
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7687n100
Supporting Variantsnssv3697546
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)nsv1053252
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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