A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2391767



Internal ID17781827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:310300..320019hg38UCSC Ensembl
Innerchr6:310300..320019hg19UCSC Ensembl
Innerchr6:255300..265019hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg389720
hg199720
hg189720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv969342
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)nssv2391767
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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