A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2563733



Internal ID17521501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97698069..97704083hg38UCSC Ensembl
Innerchr9:100460351..100466365hg19UCSC Ensembl
Innerchr9:99500172..99506186hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386015
hg196015
hg186015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972792
Supporting Variants
SamplesHGDP01284
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2563733
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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