A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566974



Internal ID20940045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122739950..122740177hg38UCSC Ensembl
chr5:122075645..122075872hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566974
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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