A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1847995



Internal ID17390098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45902056..45909652hg38UCSC Ensembl
Innerchr10:51686174..51693770hg19UCSC Ensembl
Innerchr10:51356180..51363776hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg387597
hg197597
hg187597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv947996
Supporting Variants
SamplesHGDP00456
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)nssv1847995
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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