A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902460



Internal ID22677619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6313771..6313831hg38UCSC Ensembl
chr5:6313884..6313944hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418194
Samples
Known GenesFLJ33360
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902460
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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