A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682051



Internal ID15072017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162060428..162778735hg38UCSC Ensembl
Innerchr6:162481460..163199767hg19UCSC Ensembl
Innerchr6:162401450..163119757hg18UCSC Ensembl
Innerchr6:162451871..163170178hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38718308
hg19718308
hg18718308
hg17718308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517562
Supporting Variants
Samples
Known GenesPACRG, PARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682051
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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