A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500565



Internal ID20873792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88513782..88514098hg38UCSC Ensembl
chr15:89057013..89057329hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027001
Samples
Known GenesDET1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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