A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504898



Internal ID18803179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4215479..4325567hg38UCSC Ensembl
Innerchr11:4236709..4346797hg19UCSC Ensembl
Innerchr11:4193285..4303373hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38110089
hg19110089
hg18110089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038465
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)nssv3504898
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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