A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567088



Internal ID20940159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166716051..166716779hg38UCSC Ensembl
chr5:166143056..166143784hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268135
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567088
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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