A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661453



Internal ID15398105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:165463943..165487636hg38UCSC Ensembl
Innerchr6:165877431..165901124hg19UCSC Ensembl
Innerchr6:165797421..165821114hg18UCSC Ensembl
Innerchr6:165847842..165871535hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3823694
hg1923694
hg1823694
hg1723694
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)nssv661453
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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