A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516338



Internal ID15096945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:33533389..33555164hg38UCSC Ensembl
Innerchr2:33758456..33780231hg19UCSC Ensembl
Innerchr2:33611960..33633735hg18UCSC Ensembl
Innerchr2:33670107..33691882hg17UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3821776
hg1921776
hg1821776
hg1721776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668355, nssv673029, nssv671643, nssv686069, nssv662625, nssv660562, nssv667684, nssv682327, nssv661187, nssv663151, nssv683321, nssv656030, nssv687715, nssv681597, nssv681284, nssv687561, nssv668701, nssv669532, nssv692651, nssv670556, nssv672626
Samples
Known GenesRASGRP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516338
Frequency
Sample Size2026
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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