A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027413



Internal ID20594453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91343291..91348469hg38UCSC Ensembl
chr15:91886521..91891699hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385179
hg195179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508396
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027413
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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