A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559327



Internal ID20932398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155353794..155354300hg38UCSC Ensembl
chr5:154733354..154733860hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268771
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559327
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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