A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027905



Internal ID20594945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96541889..96553206hg38UCSC Ensembl
chr15:97085119..97096436hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3811318
hg1911318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505941
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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