A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493644



Internal ID22551573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:178010981..178016631hg38UCSC Ensembl
chr4:178932135..178937785hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg385651
hg195651
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838715
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493644
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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