A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2397533



Internal ID17743312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26634715..26638680hg38UCSC Ensembl
Innerchr6:26634943..26638908hg19UCSC Ensembl
Innerchr6:26742922..26746887hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg383966
hg193966
hg183966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv965691
Supporting Variants
SamplesHGDP00456
Known GenesZNF322
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2397533
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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