A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1773087



Internal ID17878924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:83132401..83164708hg38UCSC Ensembl
Innerchr1:83598084..83630391hg19UCSC Ensembl
Innerchr1:83370672..83402979hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3832308
hg1932308
hg1832308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv946026
Supporting Variants
SamplesHGDP01307
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)nssv1773087
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