A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1846382



Internal ID17522572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45863213..45894478hg38UCSC Ensembl
Innerchr10:46358661..46389926hg19UCSC Ensembl
Innerchr10:45678667..45709932hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3831266
hg1931266
hg1831266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv947918
Supporting Variants
SamplesHGDP01284
Known Genes
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)nssv1846382
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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