A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494934



Internal ID272062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34059041..34059166hg38UCSC Ensembl
chr15:34351242..34351367hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700467
Samples
Known GenesCHRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494934
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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