A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18125877



Internal ID20692917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14334157..14334489hg38UCSC Ensembl
chr5:14334266..14334598hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380360
Supporting Variants
Samples
Known GenesTRIO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18125877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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