A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258096



Internal ID20825136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241626362..241626628hg38UCSC Ensembl
chr2:242565777..242566043hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546742
Supporting Variants
Samples
Known GenesTHAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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