A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10639n54



Internal ID20144063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42085013..42131633hg38UCSC Ensembl
chr6:42052751..42099371hg19UCSC Ensembl
chr6:42160729..42207349hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3846621
hg1946621
hg1846621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602990, nsv602991
SamplesNINDS_70, NINDS_65
Known GenesC6orf132
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10639n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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