A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270212



Internal ID20837252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75530807..75531593hg38UCSC Ensembl
chr5:74826632..74827418hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556225
Supporting Variants
Samples
Known GenesPOLK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270212
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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