A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2479639



Internal ID17405167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138479101..138492710hg38UCSC Ensembl
Innerchr7:138163846..138177455hg19UCSC Ensembl
Innerchr7:137814386..137827995hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3813610
hg1913610
hg1813610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv981589
Supporting Variants
SamplesHGDP00521
Known GenesTRIM24
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)nssv2479639
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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