A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046989



Internal ID18789520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90591705..91038134hg38UCSC Ensembl
Innerchr9:93353987..93800416hg19UCSC Ensembl
Innerchr9:92393807..92840237hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38446430
hg19446430
hg18446431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697544
Samples
Known GenesDIRAS2, SYK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046989
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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