A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10677n54



Internal ID19002853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57341122..60409841hg38UCSC Ensembl
chr6:57205920..57381883hg19UCSC Ensembl
chr6:57313879..57489842hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg383068720
hg19175964
hg18175964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603191, nsv603192
Samples
Known GenesPRIM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10677n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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