A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2557849



Internal ID17491886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92539232..92540093hg38UCSC Ensembl
Innerchr9:95301514..95302375hg19UCSC Ensembl
Innerchr9:94341335..94342196hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38862
hg19862
hg18862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982321
Supporting Variants
SamplesHGDP00998
Known GenesCENPP
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)nssv2557849
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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