A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507773



Internal ID284483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100203115..100203477hg38UCSC Ensembl
chr13:100855369..100855731hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17692639
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507773
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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