A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518501



Internal ID15445794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14769495..14842781hg38UCSC Ensembl
Innerchr4:14771119..14844405hg19UCSC Ensembl
Innerchr4:14380217..14453503hg18UCSC Ensembl
Innerchr4:14447388..14520674hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3873287
hg1973287
hg1873287
hg1773287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695941
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518501
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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