A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105804



Internal ID20672844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107588501..107593900hg38UCSC Ensembl
chr4:108509658..108515056hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg385400
hg195399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01142


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