A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257291



Internal ID20824331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230188871..230191904hg38UCSC Ensembl
chr2:231053587..231056620hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg383034
hg193034
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540068
Supporting Variants
Samples
Known GenesSP110
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257291
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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