A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2332877



Internal ID17534094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:113213323..113214921hg38UCSC Ensembl
Innerchr4:114134479..114136077hg19UCSC Ensembl
Innerchr4:114353928..114355526hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv966311
Supporting Variants
SamplesHGDP01307
Known GenesANK2
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)nssv2332877
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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