A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10686n54



Internal ID19002862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57904941..58453777hg38UCSC Ensembl
chr6:58231219..58780055hg19UCSC Ensembl
chr6:58339178..58888014hg18UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg38548837
hg19548837
hg18548837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603237, nsv603239
SamplesHGDP00208
Known GenesGUSBP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10686n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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