A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10486n54



Internal ID20143910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32187671..32193653hg38UCSC Ensembl
chr6:32155448..32161430hg19UCSC Ensembl
chr6:32263426..32269408hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg385983
hg195983
hg185983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602106, nsv602107, nsv602108
Samples
Known GenesGPSM3, PBX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10486n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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