A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386551



Internal ID21044104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14502444..14504619hg38UCSC Ensembl
chr5:14502553..14504728hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382176
hg192176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127978
Samples
Known GenesTRIO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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