A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023984



Internal ID20591024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43481501..43483000hg38UCSC Ensembl
chr15:43773699..43775198hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499100
Supporting Variants
Samples
Known GenesRNU6-28P, TP53BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023984
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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