A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1850405



Internal ID17795157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64169084..64170207hg38UCSC Ensembl
Innerchr10:65928845..65929968hg19UCSC Ensembl
Innerchr10:65598851..65599974hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381124
hg191124
hg181124
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948036
Supporting Variants
SamplesHGDP00778
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1850405
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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