A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1856686



Internal ID17795461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47463363..47483046hg38UCSC Ensembl
Innerchr10:48256316..48275999hg19UCSC Ensembl
Innerchr10:47876322..47896005hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3819684
hg1919684
hg1819684
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv947961
Supporting Variants
SamplesHGDP00778
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)nssv1856686
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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