A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503727



Internal ID280544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113624665..113624950hg38UCSC Ensembl
chr13:114278980..114279265hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17695575
Samples
Known GenesTFDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503727
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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