A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528686



Internal ID15455979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:164893207..165009016hg38UCSC Ensembl
Innerchr4:165814359..165930168hg19UCSC Ensembl
Innerchr4:166033809..166149618hg18UCSC Ensembl
Innerchr4:166171964..166287773hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38115810
hg19115810
hg18115810
hg17115810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705329
Samples
Known GenesFAM218A, LOC100506013, TRIM61
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528686
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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