A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1861925



Internal ID17870080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87109037..87126809hg38UCSC Ensembl
Innerchr10:88868794..88886566hg19UCSC Ensembl
Innerchr10:88858774..88876546hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3817773
hg1917773
hg1817773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv948114
Supporting Variants
SamplesHGDP01284
Known GenesFAM35A
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)nssv1861925
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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