A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490988



Internal ID22548913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25994948..26048041hg38UCSC Ensembl
chr3:26036439..26089532hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3853094
hg1953094
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836141
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490988
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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