A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503614



Internal ID280436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85961602..85974337hg38UCSC Ensembl
chr13:86535737..86548472hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3812736
hg1912736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17692501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503614
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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