A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963341



Internal ID18251896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:94075474..94077066hg38UCSC Ensembl
Innerchr3:93794318..93795910hg19UCSC Ensembl
Innerchr3:95277008..95278600hg18UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg381593
hg191593
hg181593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2288696, nssv2288697, nssv2288699, nssv2288694, nssv2288700, nssv2288692, nssv2288695, nssv2288691, nssv2288693, nssv2288698
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesNSUN3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963341
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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