A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270253



Internal ID20837293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77956786..77956962hg38UCSC Ensembl
chr5:77252610..77252786hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557584
Supporting Variants
Samples
Known GenesLOC101929154
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270253
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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