A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2334565



Internal ID17801005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:119334187..119369796hg38UCSC Ensembl
Innerchr4:120255342..120290951hg19UCSC Ensembl
Innerchr4:120474790..120510399hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3835610
hg1935610
hg1835610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv964091
Supporting Variants
SamplesHGDP00778
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2334565
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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