A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697544



Internal ID18649139
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 StatusS
Merged Variantsnsv1046989
Supporting Variants
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)nssv3697544
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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