A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492836



Internal ID22550764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:125561742..125567579hg38UCSC Ensembl
chr4:126482897..126488734hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg385838
hg195838
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837886
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492836
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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