A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484078



Internal ID22541986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27158626..27166725hg38UCSC Ensembl
chr2:27381494..27389593hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg388100
hg198100
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832598
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484078
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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