A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551794



Internal ID20924927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160946680..160947718hg38UCSC Ensembl
chr2:161803191..161804229hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg381039
hg191039
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4168n223
Supporting Variantsnssv18255756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551794
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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