A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021669



Internal ID18764203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162093609..162226212hg38UCSC Ensembl
Innerchr6:162514641..162647244hg19UCSC Ensembl
Innerchr6:162434631..162567234hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38132604
hg19132604
hg18132604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654552
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)nsv1021669
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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