A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268896



Internal ID20835936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57191256..57193431hg38UCSC Ensembl
chr5:56487083..56489258hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382176
hg192176
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559728
Supporting Variants
Samples
Known GenesGPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268896
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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