A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18124220



Internal ID20691260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107387779..107388523hg38UCSC Ensembl
chr5:106723480..106724224hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407695
Supporting Variants
Samples
Known GenesEFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18124220
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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