A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024094



Internal ID20591134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38314958..38315701hg38UCSC Ensembl
chr15:38607159..38607902hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503700
Supporting Variants
Samples
Known GenesSPRED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024094
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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