A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026373



Internal ID20593413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71111421..71340981hg38UCSC Ensembl
chr15:71403760..71633320hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38229561
hg19229561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498322
Supporting Variants
Samples
Known GenesCT62, THSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026373
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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