A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109063



Internal ID20676103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122458295..122458983hg38UCSC Ensembl
chr4:123379450..123380138hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382259
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109063
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00087


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