A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1851032



Internal ID17869492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64823851..64826766hg38UCSC Ensembl
Innerchr10:66583608..66586523hg19UCSC Ensembl
Innerchr10:66253614..66256529hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382916
hg192916
hg182916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948037
Supporting Variants
SamplesHGDP01284
Known GenesANXA2P3
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)nssv1851032
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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