A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967046



Internal ID18602275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:101414352..101415562hg38UCSC Ensembl
Innerchr3:101133196..101134406hg19UCSC Ensembl
Innerchr3:102615886..102617096hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg381211
hg191211
hg181211
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2289867, nssv2289870, nssv2289864, nssv2289872, nssv2289871, nssv2289868, nssv2289873, nssv2289866, nssv2289865, nssv2289869
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSENP7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967046
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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