A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10631n54



Internal ID22778526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35790295..35797962hg38UCSC Ensembl
chr6:35758072..35765739hg19UCSC Ensembl
chr6:35866050..35873717hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg387668
hg197668
hg187668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602937, nsv602936
Samples
Known GenesCLPS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10631n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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