A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2138107



Internal ID17501706
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 StatusS
Merged Variantsnsv960801
Supporting Variants
SamplesHGDP01029
Known GenesCYP4F11
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2138107
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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