A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1877745



Internal ID17532782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14277966..14279466hg38UCSC Ensembl
Innerchr11:14299512..14301012hg19UCSC Ensembl
Innerchr11:14256088..14257588hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381501
hg191501
hg181501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv975887
Supporting Variants
SamplesHGDP01307
Known GenesRRAS2
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)nssv1877745
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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