A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2528121



Internal ID17784969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33785534..33814266hg38UCSC Ensembl
Innerchr9:33785532..33814264hg19UCSC Ensembl
Innerchr9:33775532..33804264hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3828733
hg1928733
hg1828733
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968608
Supporting Variants
SamplesHGDP00665
Known GenesPRSS3
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)nssv2528121
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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