A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1892945



Internal ID17738812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63327501..63342222hg38UCSC Ensembl
Innerchr11:63094973..63109694hg19UCSC Ensembl
Innerchr11:62851549..62866270hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3814722
hg1914722
hg1814722
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975939
Supporting Variants
SamplesHGDP00456
Known GenesMIR3680-1, MIR3680-2
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)nssv1892945
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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