A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669906



Internal ID15406558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25552889..25573915hg38UCSC Ensembl
Innerchr4:25554511..25575537hg19UCSC Ensembl
Innerchr4:25163609..25184635hg18UCSC Ensembl
Innerchr4:25230780..25251806hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3821027
hg1921027
hg1821027
hg1721027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517048
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669906
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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