A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117796



Internal ID20684836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45955176..45957574hg38UCSC Ensembl
chr4:45957193..45959591hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg382399
hg192399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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