A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027785



Internal ID20594825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86014424..86018183hg38UCSC Ensembl
chr15:86557655..86561414hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg383760
hg193760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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