A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526871



Internal ID15454164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:105829057..105829871hg38UCSC Ensembl
Innerchr4:106750214..106751028hg19UCSC Ensembl
Innerchr4:106969663..106970477hg18UCSC Ensembl
Innerchr4:107107818..107108632hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38815
hg19815
hg18815
hg17815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703229
Samples
Known GenesGSTCD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526871
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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