A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982411



Internal ID18617606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65257657..65262060hg38UCSC Ensembl
Innerchr9:42740371..42744875hg19UCSC Ensembl
Innerchr9:42730367..42734871hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg384404
hg194505
hg184505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2730009, nssv2730006, nssv2730012, nssv2730014, nssv2730010, nssv2730015, nssv2730007, nssv2730011, nssv2730013, nssv2730008
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)nsv982411
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