A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1870185



Internal ID17746500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124410012..124413159hg38UCSC Ensembl
Innerchr10:126098581..126101728hg19UCSC Ensembl
Innerchr10:126088571..126091718hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383148
hg193148
hg183148
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948214
Supporting Variants
SamplesHGDP00521
Known GenesOAT
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)nssv1870185
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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