A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267993



Internal ID20835033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:144482511..144482966hg38UCSC Ensembl
chr5:143862074..143862529hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562227
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267993
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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