A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507759



Internal ID284471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28473346..28473447hg38UCSC Ensembl
chr13:29047483..29047584hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686485
Samples
Known GenesFLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507759
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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