A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562481



Internal ID20935552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152741500..152768082hg38UCSC Ensembl
chr5:152121060..152147642hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3826583
hg1926583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562481
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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