A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11019n54



Internal ID20144443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162331661..162468943hg38UCSC Ensembl
chr6:162752693..162889975hg19UCSC Ensembl
chr6:162672683..162809965hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38137283
hg19137283
hg18137283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605156, nsv605149
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11019n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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