A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520078



Internal ID15100685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161393875..161438978hg38UCSC Ensembl
Innerchr6:161814907..161860010hg19UCSC Ensembl
Innerchr6:161734897..161780000hg18UCSC Ensembl
Innerchr6:161785318..161830421hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3845104
hg1945104
hg1845104
hg1745104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673608, nssv660546
Samples
Known GenesPARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520078
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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