A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255816



Internal ID20822857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164548906..164549869hg38UCSC Ensembl
chr2:165405416..165406379hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544675
Supporting Variants
Samples
Known GenesGRB14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255816
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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