A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605114



Internal ID16045837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162183601..162190971hg38UCSC Ensembl
Innerchr6:162604633..162612003hg19UCSC Ensembl
Innerchr6:162524623..162531993hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg387371
hg197371
hg187371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075517
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605114
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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