A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18114441



Internal ID20681481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16398147..16414546hg38UCSC Ensembl
chr4:16399770..16416169hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3816400
hg1916400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18114441
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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