A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605070



Internal ID16392479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161567735..161698925hg38UCSC Ensembl
Innerchr6:161988767..162119957hg19UCSC Ensembl
Innerchr6:161908757..162039947hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38131191
hg19131191
hg18131191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075379
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605070
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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