A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527433



Internal ID15454726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:135502662..135506407hg38UCSC Ensembl
Innerchr3:135221504..135225249hg19UCSC Ensembl
Innerchr3:136704194..136707939hg18UCSC Ensembl
Innerchr3:136704202..136707947hg17UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg383746
hg193746
hg183746
hg173746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703872
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527433
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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