A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019976



Internal ID18762511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162420341..162501274hg38UCSC Ensembl
Innerchr6:162841373..162922306hg19UCSC Ensembl
Innerchr6:162761363..162842296hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3880934
hg1980934
hg1880934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655354
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)nsv1019976
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