A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2556964



Internal ID17777331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90731930..90752459hg38UCSC Ensembl
Innerchr9:93494212..93514741hg19UCSC Ensembl
Innerchr9:92534032..92554562hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3820530
hg1920530
hg1820531
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968727
Supporting Variants
SamplesHGDP00665
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)nssv2556964
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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