A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024832



Internal ID20591872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55342493..55343080hg38UCSC Ensembl
chr15:55634691..55635278hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496225
Supporting Variants
Samples
Known GenesPIGB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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