A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1895741



Internal ID17747324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:74744494..74746135hg38UCSC Ensembl
Innerchr11:74455539..74457180hg19UCSC Ensembl
Innerchr11:74133187..74134828hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381642
hg191642
hg181642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972045
Supporting Variants
SamplesHGDP00521
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)nssv1895741
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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