A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968740



Internal ID18603968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:100175426..100176219hg38UCSC Ensembl
Innerchr9:102937708..102938501hg19UCSC Ensembl
Innerchr9:101977529..101978322hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38794
hg19794
hg18794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2562403, nssv2562397, nssv2562402, nssv2562400, nssv2562399, nssv2562394, nssv2562396, nssv2562395, nssv2562401, nssv2562398
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesINVS
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968740
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