A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1843946



Internal ID17745304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45186984..45199552hg38UCSC Ensembl
Innerchr10:45682432..45695000hg19UCSC Ensembl
Innerchr10:45002438..45015006hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3812569
hg1912569
hg1812569
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947907
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)nssv1843946
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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