A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982350



Internal ID18617545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130651132..130653017hg38UCSC Ensembl
Innerchr9:133526519..133528404hg19UCSC Ensembl
Innerchr9:132516340..132518225hg18UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg381886
hg191886
hg181886
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2567822, nssv2567813, nssv2567818, nssv2567817, nssv2567814, nssv2567819, nssv2567815, nssv2567820, nssv2567821, nssv2567816
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982350
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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