A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1837795



Internal ID17745022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28898310..28900237hg38UCSC Ensembl
Innerchr10:29187239..29189166hg19UCSC Ensembl
Innerchr10:29227245..29229172hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381928
hg191928
hg181928
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947798
Supporting Variants
SamplesHGDP00521
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)nssv1837795
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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