A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1882754



Internal ID17738392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37725858..37726358hg38UCSC Ensembl
Innerchr11:37747408..37747908hg19UCSC Ensembl
Innerchr11:37703984..37704484hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975905
Supporting Variants
SamplesHGDP00456
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)nssv1882754
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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