A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549155



Internal ID20922323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55278776..55280630hg38UCSC Ensembl
chr3:55312804..55314658hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381855
hg191855
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549155
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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