A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1833012



Internal ID17827323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8514103..8515549hg38UCSC Ensembl
Innerchr10:8556066..8557512hg19UCSC Ensembl
Innerchr10:8596072..8597518hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381447
hg191447
hg181447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947734
Supporting Variants
SamplesHGDP00998
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)nssv1833012
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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