A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10257n54



Internal ID20143681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165391..311938hg38UCSC Ensembl
chr6:165391..311938hg19UCSC Ensembl
chr6:110391..256938hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38146548
hg19146548
hg18146548
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600740, nsv600736
SamplesNINDS_15
Known GenesDUSP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10257n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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