A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513881



Internal ID290390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100526143..100526490hg38UCSC Ensembl
chr14:100992480..100992827hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698804
Samples
Known GenesWDR25
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513881
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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