A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1864677



Internal ID17737562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97307959..97312391hg38UCSC Ensembl
Innerchr10:99067716..99072148hg19UCSC Ensembl
Innerchr10:99057706..99062138hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg384433
hg194433
hg184433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948156
Supporting Variants
SamplesHGDP00456
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)nssv1864677
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