A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1861596



Internal ID17828759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87430828..87500508hg38UCSC Ensembl
Innerchr10:89190585..89260265hg19UCSC Ensembl
Innerchr10:89180565..89250245hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3869681
hg1969681
hg1869681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv948126
Supporting Variants
SamplesHGDP00998
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)nssv1861596
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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