A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515139



Internal ID20888497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86945377..86960387hg38UCSC Ensembl
chr15:87488608..87503618hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3815011
hg1915011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027858
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515139
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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