A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112678



Internal ID20679718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165807134..165807743hg38UCSC Ensembl
chr4:166728286..166728895hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385839
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112678
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00056


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