A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516094



Internal ID18814375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133926415..133954738hg38UCSC Ensembl
Innerchr11:133796310..133824633hg19UCSC Ensembl
Innerchr11:133301520..133329843hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3828324
hg1928324
hg1828324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044409
Supporting Variants
Samples
Known GenesIGSF9B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3516094
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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