A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1844874



Internal ID17497862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46375720..46397324hg38UCSC Ensembl
Innerchr10:47152438..47174050hg19UCSC Ensembl
Innerchr10:46572444..46594056hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3821605
hg1921613
hg1821613
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv947932
Supporting Variants
SamplesHGDP01029
Known GenesANXA8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1844874
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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