A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257588



Internal ID20824628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28867443..28867619hg38UCSC Ensembl
chr2:29090309..29090485hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551405
Supporting Variants
Samples
Known GenesTRMT61B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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