A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105802



Internal ID20672843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107582502..107585462hg38UCSC Ensembl
chr4:108503659..108506619hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg382961
hg192961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391296
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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