A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10961n54



Internal ID20144385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145383037..145385252hg38UCSC Ensembl
chr6:145704173..145706388hg19UCSC Ensembl
chr6:145745866..145748081hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg382216
hg192216
hg182216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604824, nsv604826, nsv604825
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10961n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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