A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016331



Internal ID22077962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:17488456..17502521hg38UCSC Ensembl
Outerchr3:17488053..17504946hg38UCSC Ensembl
Innerchr3:17529948..17544013hg19UCSC Ensembl
Outerchr3:17529545..17546438hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3816894
hg1916894
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155954
Supporting Variants
Samples
Known GenesTBC1D5
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4016331
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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