A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119375



Internal ID20686415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6645543..6662525hg38UCSC Ensembl
chr4:6647270..6664252hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3816983
hg1916983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373895
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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