A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258213



Internal ID20825253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55066643..55069168hg38UCSC Ensembl
chr2:55293779..55296304hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg382526
hg192526
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548566
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258213
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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