A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524557



Internal ID15451850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:102645453..102675308hg38UCSC Ensembl
Innerchr3:102364297..102394152hg19UCSC Ensembl
Innerchr3:103846987..103876842hg18UCSC Ensembl
Innerchr3:103846987..103876842hg17UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3829856
hg1929856
hg1829856
hg1729856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700511
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524557
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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