A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569005



Internal ID20942076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28745485..28746700hg38UCSC Ensembl
chr5:28745592..28746807hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg381216
hg191216
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269571
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569005
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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