A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520186



Internal ID15447479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157808407..157820307hg38UCSC Ensembl
Innerchr4:158729559..158741459hg19UCSC Ensembl
Innerchr4:158949009..158960909hg18UCSC Ensembl
Innerchr4:159087164..159099064hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3811901
hg1911901
hg1811901
hg1711901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697269
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520186
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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