A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18115794



Internal ID20682834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175568607..175621774hg38UCSC Ensembl
chr4:176489758..176542925hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3853168
hg1953168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395582
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18115794
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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