A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155967



Internal ID22086472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61220164..61224739hg38UCSC Ensembl
Outerchr3:61204720..61225311hg38UCSC Ensembl
Innerchr3:61205838..61210413hg19UCSC Ensembl
Outerchr3:61190394..61210985hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3820592
hg1920592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016386
Samples
Known GenesFHIT
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155967
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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