A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975154



Internal ID18610362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:16973847..16976042hg38UCSC Ensembl
Innerchr11:16995394..16997589hg19UCSC Ensembl
Innerchr11:16951970..16954165hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382196
hg192196
hg182196
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1877167, nssv1877173, nssv1877166, nssv1877171, nssv1877168, nssv1877172, nssv1877174, nssv1877169, nssv1877170, nssv1877165
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPLEKHA7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975154
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