A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10331n54



Internal ID20143755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25451093..25451992hg38UCSC Ensembl
chr6:25451321..25452220hg19UCSC Ensembl
chr6:25559300..25560199hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38900
hg19900
hg18900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601169, nsv601170
Samples
Known GenesLRRC16A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10331n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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