A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705922



Internal ID15442574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:165471299..165479859hg38UCSC Ensembl
Innerchr6:165884787..165893347hg19UCSC Ensembl
Innerchr6:165804777..165813337hg18UCSC Ensembl
Innerchr6:165855198..165863758hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg388561
hg198561
hg188561
hg178561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516359
Supporting Variants
Samples
Known GenesPDE10A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705922
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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