A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1859042



Internal ID17845290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84081449..84085840hg38UCSC Ensembl
Innerchr10:85841205..85845596hg19UCSC Ensembl
Innerchr10:85831185..85835576hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384392
hg194392
hg184392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948106
Supporting Variants
SamplesHGDP01029
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)nssv1859042
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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