A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269200



Internal ID20836240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65723866..65724756hg38UCSC Ensembl
chr5:65019693..65020583hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571662
Supporting Variants
Samples
Known GenesNLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269200
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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