A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268006



Internal ID20835046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145890472..146010814hg38UCSC Ensembl
chr5:145270035..145390377hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38120343
hg19120343
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568288
Supporting Variants
Samples
Known GenesSH3RF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268006
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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