A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521677



Internal ID297964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68199818..68200164hg38UCSC Ensembl
chr15:68492156..68492502hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703890
Samples
Known GenesCALML4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521677
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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