A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522741



Internal ID15450034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:97952516..98136306hg38UCSC Ensembl
Innerchr4:98873667..99057457hg19UCSC Ensembl
Innerchr4:99092690..99276480hg18UCSC Ensembl
Innerchr4:99230845..99414635hg17UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38183791
hg19183791
hg18183791
hg17183791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv325n21
Supporting Variantsnssv698375
Samples
Known GenesSTPG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522741
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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