A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1076n54



Internal ID22768971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:41773083..41883666hg38UCSC Ensembl
chr10:42356543..42467126hg19UCSC Ensembl
chr10:41676549..41787132hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38110584
hg19110584
hg18110584
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550596, nsv550593
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1076n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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