A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1993937



Internal ID17472144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:88699249..88700790hg38UCSC Ensembl
Innerchr14:89165593..89167134hg19UCSC Ensembl
Innerchr14:88235346..88236887hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg381542
hg191542
hg181542
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv983848
Supporting Variants
SamplesHGDP00927
Known GenesEML5
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)nssv1993937
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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