A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1190n54



Internal ID22769085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57094024..57159139hg38UCSC Ensembl
chr10:58853784..58918899hg19UCSC Ensembl
chr10:58523790..58588905hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3865116
hg1965116
hg1865116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551107, nsv551108
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1190n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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