A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516589



Internal ID15097196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4080585..4286727hg38UCSC Ensembl
Innerchr3:4122269..4328411hg19UCSC Ensembl
Innerchr3:4097269..4303411hg18UCSC Ensembl
Innerchr3:4097269..4303411hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38206143
hg19206143
hg18206143
hg17206143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv272n21
Supporting Variantsnssv655669, nssv699824, nssv690958, nssv659854, nssv703552, nssv654390, nssv672084, nssv705750, nssv679858, nssv703873, nssv691573, nssv690683, nssv685184, nssv681510, nssv656806, nssv669408, nssv680352, nssv699540, nssv691164, nssv676488, nssv705240, nssv696901, nssv682376, nssv682087, nssv686207
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516589
Frequency
Sample Size2026
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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