A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10379n54



Internal ID22778274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31301571..31353908hg38UCSC Ensembl
chr6:31269348..31321685hg19UCSC Ensembl
chr6:31377327..31429664hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3852338
hg1952338
hg1852338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601589, nsv601659, nsv601667, nsv601519
Samples1780854065_A, 1780862403_A
Known GenesHLA-B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10379n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer