A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2546376



Internal ID17776346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66722800..66744749hg38UCSC Ensembl
Innerchr9:66060206..66082155hg19UCSC Ensembl
Innerchr9:65800026..65821975hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3821950
hg1921950
hg1821950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv972734
Supporting Variants
SamplesHGDP00542
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)nssv2546376
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