A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10717n54



Internal ID22778612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63952818..63958300hg38UCSC Ensembl
chr6:64662711..64668193hg19UCSC Ensembl
chr6:64720670..64726152hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg385483
hg195483
hg185483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603378, nsv603377
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10717n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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