A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1836418



Internal ID17868734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26935691..26946921hg38UCSC Ensembl
Innerchr10:27224620..27235850hg19UCSC Ensembl
Innerchr10:27264626..27275856hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3811231
hg1911231
hg1811231
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947784
Supporting Variants
SamplesHGDP01284
Known GenesLINC00202-1
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)nssv1836418
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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