A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542543



Internal ID20915802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160946895..160947725hg38UCSC Ensembl
chr2:161803406..161804236hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38831
hg19831
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4168n223
Supporting Variantsnssv18255757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542543
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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