A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569820



Internal ID20942891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75387089..75387422hg38UCSC Ensembl
chr5:74682914..74683247hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270206
Samples
Known GenesCOL4A3BP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569820
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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