A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10350n54



Internal ID20143774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29890188..29901207hg38UCSC Ensembl
chr6:29857965..29868984hg19UCSC Ensembl
chr6:29965944..29976963hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3811020
hg1911020
hg1811020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601301, nsv601307, nsv601302
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10350n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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