A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2547976



Internal ID17846709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62918791..62954364hg38UCSC Ensembl
Innerchr9:66574615..66610188hg19UCSC Ensembl
Innerchr9:66314435..66350008hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3835574
hg1935574
hg1835574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv972739
Supporting Variants
SamplesHGDP01029
Known Genes
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)nssv2547976
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