A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255644



Internal ID20822684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104615712..104630940hg38UCSC Ensembl
chr2:105232170..105247398hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3815229
hg1915229
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538226
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255644
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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