A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2559132



Internal ID17750853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94376780..94437874hg38UCSC Ensembl
Innerchr9:97139062..97200156hg19UCSC Ensembl
Innerchr9:96178883..96239977hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3861095
hg1961095
hg1861095
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv982324
Supporting Variants
SamplesHGDP00521
Known GenesHIATL1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2559132
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer