A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486972



Internal ID22544887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57719622..57728050hg38UCSC Ensembl
chr2:57946757..57955185hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg388429
hg198429
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486972
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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