A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11004n54



Internal ID20144428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162106599..162308349hg38UCSC Ensembl
chr6:162527631..162729381hg19UCSC Ensembl
chr6:162447621..162649371hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38201751
hg19201751
hg18201751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605077, nsv605079
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11004n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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