A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2391789



Internal ID17786216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:349825..354614hg38UCSC Ensembl
Innerchr6:349825..354614hg19UCSC Ensembl
Innerchr6:294825..299614hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg384790
hg194790
hg184790
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv981097
Supporting Variants
SamplesHGDP00665
Known GenesDUSP22
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2391789
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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