A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1862437



Internal ID17795739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89786423..89790925hg38UCSC Ensembl
Innerchr10:91546180..91550682hg19UCSC Ensembl
Innerchr10:91536160..91540662hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg384503
hg194503
hg184503
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948132
Supporting Variants
SamplesHGDP00778
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)nssv1862437
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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