A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5514692



Internal ID291186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80653852..80655686hg38UCSC Ensembl
chr15:80946193..80948027hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381835
hg191835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704460
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5514692
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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