A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021481



Internal ID18764015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162411196..162429111hg38UCSC Ensembl
Innerchr6:162832228..162850143hg19UCSC Ensembl
Innerchr6:162752218..162770133hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3817916
hg1917916
hg1817916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655353
Samples
Known GenesPARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021481
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer