A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967075



Internal ID18602304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143176597..143178944hg38UCSC Ensembl
Innerchr3:142895439..142897786hg19UCSC Ensembl
Innerchr3:144378129..144380476hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg382348
hg192348
hg182348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2298253, nssv2298254, nssv2298252, nssv2298250, nssv2298257, nssv2298256, nssv2298255, nssv2298249, nssv2298258, nssv2298251
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)nsv967075
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