A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972782



Internal ID18607998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93335667..93336793hg38UCSC Ensembl
Innerchr9:96097949..96099075hg19UCSC Ensembl
Innerchr9:95137770..95138896hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381127
hg191127
hg181127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2560087, nssv2560092, nssv2560093, nssv2560089, nssv2560094, nssv2560088, nssv2560085, nssv2560090, nssv2560091, nssv2560086
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC9orf129
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972782
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