A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1831185



Internal ID17868476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11624232..11629460hg38UCSC Ensembl
Innerchr10:11666231..11671459hg19UCSC Ensembl
Innerchr10:11706237..11711465hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385229
hg195229
hg185229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947738
Supporting Variants
SamplesHGDP01284
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)nssv1831185
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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