A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1774097



Internal ID17779576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:87448158..87452651hg38UCSC Ensembl
Innerchr1:87913841..87918334hg19UCSC Ensembl
Innerchr1:87686429..87690922hg18UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg384494
hg194494
hg184494
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv946044
Supporting Variants
SamplesHGDP00665
Known Genes
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)nssv1774097
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