A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1832784



Internal ID17744806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22224974..22226349hg38UCSC Ensembl
Innerchr10:22513903..22515278hg19UCSC Ensembl
Innerchr10:22553909..22555284hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381376
hg191376
hg181376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947766
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)nssv1832784
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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