A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969363



Internal ID18604590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26923417..27002684hg38UCSC Ensembl
Innerchr6:26891196..26970463hg19UCSC Ensembl
Innerchr6:26999175..27078442hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3879268
hg1979268
hg1879268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2398745, nssv2398737, nssv2398739, nssv2398742, nssv2398740, nssv2398741, nssv2398743, nssv2398744, nssv2398738, nssv2398736
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGUSBP2, LINC00240
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969363
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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