A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655361



Internal ID18606956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162444113..162913747hg38UCSC Ensembl
Innerchr6:162865145..163334779hg19UCSC Ensembl
Innerchr6:162785135..163254769hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38469635
hg19469635
hg18469635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015507
Supporting Variants
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)nssv3655361
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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