A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256761



Internal ID20823801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12690722..12691207hg38UCSC Ensembl
chr2:12830848..12831333hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549648
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256761
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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