A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484065



Internal ID22541973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25994460..25998419hg38UCSC Ensembl
chr2:26217329..26221288hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg383960
hg193960
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832926
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484065
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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