A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10900n54



Internal ID22778795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108289437..108292170hg38UCSC Ensembl
chr6:108610641..108613374hg19UCSC Ensembl
chr6:108717334..108720067hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382734
hg192734
hg182734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604462, nsv604458, nsv604467, nsv604457
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10900n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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