A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025396



Internal ID18767928
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 StatusM
Merged Variantsdgv6176n100
Supporting Variantsnssv3654558, nssv3749586
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)nsv1025396
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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