A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257489



Internal ID20824529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241322598..241323419hg38UCSC Ensembl
chr2:242262013..242262834hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38822
hg19822
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535753
Supporting Variants
Samples
Known GenesSEPT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257489
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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