A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527183



Internal ID303288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78177021..78177239hg38UCSC Ensembl
chr15:78469363..78469581hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702179
Samples
Known GenesACSBG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527183
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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