A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525845



Internal ID15106452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:40681959..40776145hg38UCSC Ensembl
Innerchr4:40683976..40778162hg19UCSC Ensembl
Innerchr4:40378733..40472919hg18UCSC Ensembl
Innerchr4:40524904..40619090hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3894187
hg1994187
hg1894187
hg1794187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702038
Samples
Known GenesNSUN7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525845
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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