A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10411n54



Internal ID22778306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31314853..31372298hg38UCSC Ensembl
chr6:31282630..31340075hg19UCSC Ensembl
chr6:31390609..31448054hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3857446
hg1957446
hg1857446
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601705, nsv601795, nsv601704, nsv601776, nsv601726, nsv601690, nsv601758, nsv601703, nsv601759, nsv601675, nsv601789, nsv601714
Samples
Known GenesHLA-B, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10411n54
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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