A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568634



Internal ID20941705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100585525..100588449hg38UCSC Ensembl
chr5:99921229..99924153hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg382925
hg192925
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266141
Samples
Known GenesFAM174A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568634
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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