A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255290



Internal ID20822330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156407974..156408703hg38UCSC Ensembl
chr2:157264486..157265215hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255290
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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