A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686406



Internal ID15423058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25555425..25581609hg38UCSC Ensembl
Innerchr4:25557047..25583231hg19UCSC Ensembl
Innerchr4:25166145..25192329hg18UCSC Ensembl
Innerchr4:25233316..25259500hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3826185
hg1926185
hg1826185
hg1726185
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)nssv686406
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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