A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2556402



Internal ID17776189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87771928..87773223hg38UCSC Ensembl
Innerchr9:90386843..90388138hg19UCSC Ensembl
Innerchr9:89576663..89577958hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381296
hg191296
hg181296
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972413
Supporting Variants
SamplesHGDP00542
Known GenesCTSL3P
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)nssv2556402
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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