A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573304



Internal ID20946375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67998624..67999767hg38UCSC Ensembl
chr5:67294452..67295595hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg381144
hg191144
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5782n223
Supporting Variantsnssv18266959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573304
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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