A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517888



Internal ID15445181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4949454..4978251hg38UCSC Ensembl
Innerchr3:4991139..5019936hg19UCSC Ensembl
Innerchr3:4966139..4994936hg18UCSC Ensembl
Innerchr3:4966139..4994936hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3828798
hg1928798
hg1828798
hg1728798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695296
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517888
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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