A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502201



Internal ID20875444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93118775..93142232hg38UCSC Ensembl
chr15:93662004..93685461hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3823458
hg1923458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502201
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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