A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527260



Internal ID15107867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161950673..162054402hg38UCSC Ensembl
Innerchr6:162371705..162475434hg19UCSC Ensembl
Innerchr6:162291695..162395424hg18UCSC Ensembl
Innerchr6:162342116..162445845hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38103730
hg19103730
hg18103730
hg17103730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703666
Samples
Known GenesPARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527260
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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