A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526989



Internal ID15454282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141522955..141579900hg38UCSC Ensembl
Innerchr4:142444108..142501053hg19UCSC Ensembl
Innerchr4:142663558..142720503hg18UCSC Ensembl
Innerchr4:142801713..142858658hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3856946
hg1956946
hg1856946
hg1756946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703362
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526989
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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