A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10991n54



Internal ID22778886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160839498..160858507hg38UCSC Ensembl
chr6:161260530..161279539hg19UCSC Ensembl
chr6:161180520..161199529hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3819010
hg1919010
hg1819010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605022, nsv605013, nsv605020
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10991n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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