A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268704



Internal ID20835744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150976004..150976784hg38UCSC Ensembl
chr5:150355566..150356346hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567031
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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