A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527765



Internal ID303850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47069127..47069239hg38UCSC Ensembl
chr15:47361325..47361437hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527765
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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