A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973336



Internal ID18608551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63802120..63818406hg38UCSC Ensembl
Innerchr9:68397854..68414140hg19UCSC Ensembl
Innerchr9:67887674..67903960hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3816287
hg1916287
hg1816287
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2741189, nssv2741182, nssv2741185, nssv2741188, nssv2741184, nssv2741186, nssv2741183, nssv2741190, nssv2741181, nssv2741187
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973336
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