A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258942



Internal ID20825982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70368569..70369980hg38UCSC Ensembl
chr2:70595701..70597112hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg381412
hg191412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258942
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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