A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517439



Internal ID15444732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14415880..14429763hg38UCSC Ensembl
Innerchr4:14417504..14431387hg19UCSC Ensembl
Innerchr4:14026602..14040485hg18UCSC Ensembl
Innerchr4:14093773..14107656hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3813884
hg1913884
hg1813884
hg1713884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673169, nssv652026
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517439
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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