A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1846631



Internal ID17390044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45928109..45931516hg38UCSC Ensembl
Innerchr10:46423557..46426964hg19UCSC Ensembl
Innerchr10:45743563..45747193hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383408
hg193408
hg183631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv947920
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)nssv1846631
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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