A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10711n54



Internal ID22778606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:62356335..62463388hg38UCSC Ensembl
chr6:63066240..63173293hg19UCSC Ensembl
chr6:63124199..63231252hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38107054
hg19107054
hg18107054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603350, nsv603351
SamplesNINDS_125
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10711n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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