A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027229



Internal ID20594269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84641053..84641241hg38UCSC Ensembl
chr15:85184284..85184472hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498059
Supporting Variants
Samples
Known GenesSCAND2P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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