A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1839629



Internal ID17844272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36438622..36440516hg38UCSC Ensembl
Innerchr10:36727550..36729444hg19UCSC Ensembl
Innerchr10:36767556..36769450hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381895
hg191895
hg181895
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947836
Supporting Variants
SamplesHGDP01029
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)nssv1839629
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