A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759789



Internal ID18711384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95030756..95119134hg38UCSC Ensembl
Innerchr9:97793038..97881416hg19UCSC Ensembl
Innerchr9:96832859..96921237hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3888379
hg1988379
hg1888379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038106
Supporting Variants
Samples
Known GenesC9orf3, FANCC, MIR23B, MIR24-1, MIR27B, MIR3074, MIR6081
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3759789
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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