A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972726



Internal ID18607942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41628395..41649013hg38UCSC Ensembl
Innerchr9:46097664..46118282hg19UCSC Ensembl
Innerchr9:45987660..46008278hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3820619
hg1920619
hg1820619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2540915, nssv2540920, nssv2542747, nssv2540918, nssv2540917, nssv2542748, nssv2540921, nssv2540922, nssv2540916, nssv2540919
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972726
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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