A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270218



Internal ID20837258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76377957..76416908hg38UCSC Ensembl
chr5:75673782..75712733hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3838952
hg1938952
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564143
Supporting Variants
Samples
Known GenesIQGAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270218
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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