A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451781



Internal ID229951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70995280..70998632hg38UCSC Ensembl
chr3:71044431..71047783hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg383353
hg193353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935081
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451781
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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