A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495933



Internal ID22553866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54203748..54205873hg38UCSC Ensembl
chr4:55069915..55072040hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382126
hg192126
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839367
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495933
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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