A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256997



Internal ID20824037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19116772..19179731hg38UCSC Ensembl
chr2:19316533..19379492hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3862960
hg1962960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555253
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256997
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0001


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