A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10897n54



Internal ID22778792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107114286..107115306hg38UCSC Ensembl
chr6:107435490..107436510hg19UCSC Ensembl
chr6:107542183..107543203hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381021
hg191021
hg181021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604447, nsv604444
Samples
Known GenesBEND3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10897n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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