A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129455



Internal ID20696495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15603501..15606400hg38UCSC Ensembl
chr5:15603610..15606509hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6386302
Supporting Variants
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00054


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