A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558878



Internal ID331930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41206275..41206310hg38UCSC Ensembl
chr15:41498473..41498508hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701101
Samples
Known GenesEXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558878
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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