A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10454n54



Internal ID20143878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31387541..31489856hg38UCSC Ensembl
chr6:31355318..31457633hg19UCSC Ensembl
chr6:31463297..31565612hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38102316
hg19102316
hg18102316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601887, nsv601903, nsv601902, nsv601885, nsv601905, nsv601891, nsv601877, nsv601888, nsv601906
SamplesNINDS_192
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10454n54
Frequency
Sample Size17421
Observed Gain21
Observed Loss0
Observed Complex0
Frequencyn/a


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