A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016439



Internal ID18758974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162255161..162657210hg38UCSC Ensembl
Innerchr6:162676193..163078242hg19UCSC Ensembl
Innerchr6:162596183..162998232hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38402050
hg19402050
hg18402050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6178n100
Supporting Variantsnssv3654571
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)nsv1016439
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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