A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1864774



Internal ID17737564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97391206..97393664hg38UCSC Ensembl
Innerchr10:99150963..99153421hg19UCSC Ensembl
Innerchr10:99140953..99143411hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382459
hg192459
hg182459
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948157
Supporting Variants
SamplesHGDP00456
Known GenesRRP12
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)nssv1864774
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