A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520625



Internal ID15101232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:78081501..78150634hg38UCSC Ensembl
Innerchr4:79002655..79071788hg19UCSC Ensembl
Innerchr4:79221679..79290812hg18UCSC Ensembl
Innerchr4:79359834..79428967hg17UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3869134
hg1969134
hg1869134
hg1769134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697524
Samples
Known GenesFRAS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520625
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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