A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1863861



Internal ID17845260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92114843..92116895hg38UCSC Ensembl
Innerchr10:93874600..93876652hg19UCSC Ensembl
Innerchr10:93864580..93866632hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg382053
hg192053
hg182053
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv948136
Supporting Variants
SamplesHGDP01029
Known GenesCPEB3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1863861
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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