A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11027n54



Internal ID20144451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163414144..163415657hg38UCSC Ensembl
chr6:163835176..163836689hg19UCSC Ensembl
chr6:163755166..163756679hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381514
hg191514
hg181514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605208, nsv605207
Samples
Known GenesQKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11027n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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