A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1846026



Internal ID17778380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45722576..45748192hg38UCSC Ensembl
Innerchr10:46218024..46243640hg19UCSC Ensembl
Innerchr10:45538030..45563646hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3825617
hg1925617
hg1825617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv947914
Supporting Variants
SamplesHGDP00665
Known GenesFAM21C
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)nssv1846026
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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