A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495135



Internal ID22553068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43860449..43867026hg38UCSC Ensembl
chr4:43862466..43869043hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg386578
hg196578
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839630
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495135
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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