A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669285



Internal ID15405937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152945141..152975383hg38UCSC Ensembl
Innerchr5:152324701..152354943hg19UCSC Ensembl
Innerchr5:152304894..152335136hg18UCSC Ensembl
Innerchr5:152304894..152335136hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3830243
hg1930243
hg1830243
hg1730243
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516577
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669285
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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