A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1857940



Internal ID17745950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79508068..79548153hg38UCSC Ensembl
Innerchr10:81267824..81307909hg19UCSC Ensembl
Innerchr10:80937830..80977915hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3840086
hg1940086
hg1840086
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948082
Supporting Variants
SamplesHGDP00521
Known GenesEIF5AL1
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)nssv1857940
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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