A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511657



Internal ID288229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25755585..25761321hg38UCSC Ensembl
chr15:26000732..26006468hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg385737
hg195737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698581
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511657
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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