A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507908



Internal ID284613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37576736..37576814hg38UCSC Ensembl
chr13:38150873..38150951hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686955
Samples
Known GenesPOSTN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507908
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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