A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257746



Internal ID20824786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202571689..202572200hg38UCSC Ensembl
chr2:203436412..203436923hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257746
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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