A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960801



Internal ID18249362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15922084..15924858hg38UCSC Ensembl
Innerchr19:16032894..16035668hg19UCSC Ensembl
Innerchr19:15893894..15896668hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382775
hg192775
hg182775
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2138103, nssv2138106, nssv2138102, nssv2138107, nssv2138104, nssv2138108, nssv2138100, nssv2138101, nssv2138105, nssv2138109
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCYP4F11
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960801
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