A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2551069



Internal ID17739904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68220553..68238951hg38UCSC Ensembl
Innerchr9:70835469..70853867hg19UCSC Ensembl
Innerchr9:70025069..70043687hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3818399
hg1918399
hg1818619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv968702
Supporting Variants
SamplesHGDP00456
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2551069
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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