A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749586



Internal ID18701181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162168986..162762531hg38UCSC Ensembl
Innerchr6:162590018..163183563hg19UCSC Ensembl
Innerchr6:162510008..163103553hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38593546
hg19593546
hg18593546
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025396
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)nssv3749586
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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