A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512319



Internal ID288875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37319409..37322218hg38UCSC Ensembl
chr15:37611610..37614419hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382810
hg192810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv168n206
Supporting Variantsnssv17701487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512319
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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