A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1871455



Internal ID17796169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1016368..1042943hg38UCSC Ensembl
Innerchr11:1016368..1042943hg19UCSC Ensembl
Innerchr11:1006368..1032943hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3826576
hg1926576
hg1826576
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975870
Supporting Variants
SamplesHGDP00778
Known GenesMUC6
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)nssv1871455
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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