A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540737



Internal ID315452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21936719..21936724hg38UCSC Ensembl
chr8:21794230..21794235hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17010212
Samples
Known GenesXPO7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540737
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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