A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549742



Internal ID20922897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31381758..31389558hg38UCSC Ensembl
chr3:31423250..31431050hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg387801
hg197801
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549742
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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