A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565878



Internal ID20938949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100460132..101555680hg38UCSC Ensembl
chr5:99795836..100891384hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg381095549
hg191095549
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266140
Samples
Known GenesFAM174A, ST8SIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565878
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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