A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107767



Internal ID20674807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109691190..109691947hg38UCSC Ensembl
chr4:110612346..110613103hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385288
Supporting Variants
Samples
Known GenesCASP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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