A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972808



Internal ID18608024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128272628..128276957hg38UCSC Ensembl
Innerchr9:131034907..131039236hg19UCSC Ensembl
Innerchr9:130074728..130079057hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384330
hg194330
hg184330
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2567655, nssv2567652, nssv2567656, nssv2567649, nssv2567650, nssv2567651, nssv2567654, nssv2567658, nssv2567657, nssv2567653
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGOLGA2, SWI5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972808
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