A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2526333



Internal ID17399271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33381481..33395414hg38UCSC Ensembl
Innerchr9:33381479..33395412hg19UCSC Ensembl
Innerchr9:33371479..33385412hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3813934
hg1913934
hg1813934
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv972661
Supporting Variants
SamplesHGDP00521
Known GenesAQP7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2526333
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