A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544553



Internal ID20917792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5383538..5413862hg38UCSC Ensembl
chr2:5523671..5553995hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3830325
hg1930325
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544553
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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