A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496390



Internal ID20869592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64794121..64795988hg38UCSC Ensembl
chr15:65086320..65088187hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381868
hg191868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025698
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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