A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568937



Internal ID20942008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112855244..112856148hg38UCSC Ensembl
chr5:112190941..112191845hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568937
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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