A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1844432



Internal ID17794859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43787601..43790637hg38UCSC Ensembl
Innerchr10:44283049..44286085hg19UCSC Ensembl
Innerchr10:43603055..43606091hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383037
hg193037
hg183037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947899
Supporting Variants
SamplesHGDP00778
Known GenesHNRNPA3P1
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)nssv1844432
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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