A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489381



Internal ID22547300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236799399..236816219hg38UCSC Ensembl
chr2:237708042..237724862hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3816821
hg1916821
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832258
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489381
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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