A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515896



Internal ID15442953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85829000..85863447hg38UCSC Ensembl
Innerchr6:86538718..86573165hg19UCSC Ensembl
Innerchr6:86595437..86629884hg18UCSC Ensembl
Innerchr6:86595437..86629884hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3834448
hg1934448
hg1834448
hg1734448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv388n21
Supporting Variantsnssv679449, nssv664173, nssv689927, nssv683791, nssv675649, nssv692178, nssv652275, nssv653394, nssv686536, nssv661086, nssv674321, nssv693116, nssv668861, nssv679098, nssv663991, nssv656662, nssv685316, nssv704936, nssv671950, nssv665137, nssv669313, nssv682892, nssv663309, nssv692500, nssv659787, nssv685061, nssv693173, nssv664341, nssv668979, nssv693300, nssv673882, nssv669522, nssv663344, nssv662548, nssv679030, nssv654454, nssv670745, nssv703963, nssv692387, nssv681384, nssv680380, nssv681750, nssv667453, nssv660945, nssv699851, nssv685917, nssv676186, nssv676765, nssv659843, nssv671157, nssv661642, nssv689524
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515896
Frequency
Sample Size2026
Observed Gain0
Observed Loss52
Observed Complex0
Frequencyn/a


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