A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025439



Internal ID20592479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67022854..67029555hg38UCSC Ensembl
chr15:67315192..67321893hg19UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg386702
hg196702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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