A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026490



Internal ID18769022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162712401..163284676hg38UCSC Ensembl
Innerchr6:163133433..163705708hg19UCSC Ensembl
Innerchr6:163053423..163625698hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38572276
hg19572276
hg18572276
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655389
Samples
Known GenesPACRG, PARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026490
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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