A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972416



Internal ID18607632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88398539..88415241hg38UCSC Ensembl
Innerchr9:91013454..91030156hg19UCSC Ensembl
Innerchr9:90203274..90219976hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3816703
hg1916703
hg1816703
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2558278, nssv2558283, nssv2558280, nssv2558285, nssv2558286, nssv2558287, nssv2558279, nssv2558282, nssv2558284, nssv2558281
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSPIN1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972416
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer