A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508614



Internal ID18806895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134963950..135074876hg38UCSC Ensembl
Innerchr11:134833844..134944770hg19UCSC Ensembl
Innerchr11:134339054..134449982hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38110927
hg19110927
hg18110929
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052345
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3508614
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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