A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511026



Internal ID18462621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:19208331..19226721hg38UCSC Ensembl
Innerchr11:19229878..19248268hg19UCSC Ensembl
Innerchr11:19186454..19204844hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3818391
hg1918391
hg1818391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041249
Supporting Variants
Samples
Known GenesCSRP3, E2F8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511026
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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