A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3364n54



Internal ID22771259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101239108..101253794hg38UCSC Ensembl
chr13:101891459..101906145hg19UCSC Ensembl
chr13:100689460..100704146hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3814687
hg1914687
hg1814687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562961, nsv562968
Samples
Known GenesNALCN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3364n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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