A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1985642



Internal ID17880812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39384692..39386501hg38UCSC Ensembl
Innerchr14:39853896..39855705hg19UCSC Ensembl
Innerchr14:38923647..38925456hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg381810
hg191810
hg181810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv983818
Supporting Variants
SamplesHGDP01307
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)nssv1985642
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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