A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967804



Internal ID18603032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:158277710..158280238hg38UCSC Ensembl
Innerchr4:159198862..159201390hg19UCSC Ensembl
Innerchr4:159418312..159420840hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382529
hg192529
hg182529
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2339981, nssv2339989, nssv2339986, nssv2339982, nssv2339988, nssv2339983, nssv2339985, nssv2339984, nssv2339987, nssv2339980
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)nsv967804
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