A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1766628



Internal ID17399210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25260030..25293460hg38UCSC Ensembl
Innerchr1:25586521..25619951hg19UCSC Ensembl
Innerchr1:25459108..25492538hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3833431
hg1933431
hg1833431
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv945831
Supporting Variants
SamplesHGDP00521
Known GenesRHD
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)nssv1766628
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