A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1854221



Internal ID17811822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69023222..69025927hg38UCSC Ensembl
Innerchr10:70782978..70785683hg19UCSC Ensembl
Innerchr10:70452984..70455689hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382706
hg192706
hg182706
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948054
Supporting Variants
SamplesHGDP00927
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)nssv1854221
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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