A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493386



Internal ID22551315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25282602..25284601hg38UCSC Ensembl
chr4:25284224..25286223hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838645
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493386
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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