A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518102



Internal ID15445395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16384826..16408671hg38UCSC Ensembl
Innerchr4:16386449..16410294hg19UCSC Ensembl
Innerchr4:15995547..16019392hg18UCSC Ensembl
Innerchr4:16062718..16086563hg17UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3823846
hg1923846
hg1823846
hg1723846
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695515
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518102
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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