A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548559



Internal ID20921742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54895159..54895881hg38UCSC Ensembl
chr1:55360832..55361554hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249815
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548559
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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