A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268739



Internal ID20835779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154074932..154075571hg38UCSC Ensembl
chr5:153454492..153455131hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572609
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268739
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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