A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2548234



Internal ID17747991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63252863..63311783hg38UCSC Ensembl
Innerchr9:67207835..67266755hg19UCSC Ensembl
Innerchr9:66897405..66956575hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3858921
hg1958921
hg1859171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv982282
Supporting Variants
SamplesHGDP00521
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2548234
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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