A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2274925



Internal ID17769875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15879271..15881373hg38UCSC Ensembl
Innerchr3:15920778..15922880hg19UCSC Ensembl
Innerchr3:15895782..15897884hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382103
hg192103
hg182103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv966991
Supporting Variants
SamplesHGDP00542
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)nssv2274925
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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