A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566913



Internal ID20939984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180809194..180840700hg38UCSC Ensembl
chr5:180236194..180267700hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3831507
hg1931507
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268244
Samples
Known GenesHEIH, LINC00847, MGAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566913
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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