A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10457n54



Internal ID20143881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31392612..31469528hg38UCSC Ensembl
chr6:31360389..31437305hg19UCSC Ensembl
chr6:31468368..31545284hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3876917
hg1976917
hg1876917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601896, nsv601917
Samples
Known GenesHCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10457n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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