A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1895433



Internal ID17826377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71584255..71604480hg38UCSC Ensembl
Innerchr11:71295301..71315526hg19UCSC Ensembl
Innerchr11:70972949..70993174hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3820226
hg1920226
hg1820226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975946
Supporting Variants
SamplesHGDP00998
Known Genes
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)nssv1895433
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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