A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982399



Internal ID18617594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40254521..40257239hg38UCSC Ensembl
Innerchr9:42399539..42402257hg19UCSC Ensembl
Innerchr9:42389535..42392253hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg382719
hg192719
hg182719
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv85n82
Supporting Variantsnssv2728542, nssv2728538, nssv2728539, nssv2728537, nssv2728536, nssv2728540, nssv2728535, nssv2728534, nssv2728541, nssv2728533
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982399
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