A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963311



Internal ID18598552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:40252277..40253482hg38UCSC Ensembl
Innerchr3:40293768..40294973hg19UCSC Ensembl
Innerchr3:40268772..40269977hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg381206
hg191206
hg181206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2276866, nssv2276862, nssv2276868, nssv2276867, nssv2276863, nssv2276869, nssv2276860, nssv2276864, nssv2276865, nssv2276861
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesEIF1B-AS1, MYRIP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963311
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