A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022215



Internal ID20589256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95680956..95689157hg38UCSC Ensembl
chr14:96147293..96155494hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg388202
hg198202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503195
Supporting Variants
Samples
Known GenesTCL1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022215
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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