A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258528



Internal ID20825568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206298707..206299608hg38UCSC Ensembl
chr2:207163431..207164332hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542595
Supporting Variants
Samples
Known GenesZDBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258528
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00055


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