A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982249



Internal ID18617444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42807809..42831967hg38UCSC Ensembl
Innerchr9:44139152..44163310hg19UCSC Ensembl
Innerchr9:44079148..44103306hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3824159
hg1924159
hg1824159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2538976, nssv2538979, nssv2538977, nssv2538980, nssv2538978, nssv2538981, nssv2538985, nssv2538982, nssv2538983, nssv2538984
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982249
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