A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526090



Internal ID15106697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161888092..161902965hg38UCSC Ensembl
Innerchr6:162309124..162323997hg19UCSC Ensembl
Innerchr6:162229114..162243987hg18UCSC Ensembl
Innerchr6:162279535..162294408hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3814874
hg1914874
hg1814874
hg1714874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702336
Samples
Known GenesPARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526090
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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