A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170015



Internal ID21314076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81142073..81168151hg38UCSC Ensembl
Outerchr11:81138533..81170083hg38UCSC Ensembl
Innerchr11:80853116..80879194hg19UCSC Ensembl
Outerchr11:80849576..80881126hg19UCSC Ensembl
Innerchr11:80530764..80556842hg18UCSC Ensembl
Outerchr11:80527224..80558774hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3831551
hg1931551
hg1831551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246112
SamplesNGO_32
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170015
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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