A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695282



Internal ID18993563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130604380..130643160hg38UCSC Ensembl
Innerchr9:133479767..133518547hg19UCSC Ensembl
Innerchr9:132469588..132508368hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3838781
hg1938781
hg1838781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054840
Supporting Variants
Samples
Known GenesFUBP3, MIR6856
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695282
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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