A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255293



Internal ID20822333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156415200..156415580hg38UCSC Ensembl
chr2:157271712..157272092hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536799
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255293
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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