A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026455



Internal ID20593495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81257632..81265726hg38UCSC Ensembl
chr15:81549973..81558067hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg388095
hg198095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505299
Supporting Variants
Samples
Known GenesIL16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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