A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513280



Internal ID289808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26006802..26014400hg38UCSC Ensembl
chr15:26251949..26259547hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg387599
hg197599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698594
Samples
Known GenesLOC100128714
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513280
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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