A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1844055



Internal ID17481189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46583673..46650504hg38UCSC Ensembl
Innerchr10:46899113..46965944hg19UCSC Ensembl
Innerchr10:46319119..46385950hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3866832
hg1966832
hg1866832
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv947928
Supporting Variants
SamplesHGDP00998
Known GenesFAM35BP, SYT15
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)nssv1844055
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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