A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272462



Internal ID20839502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138531610..138533555hg38UCSC Ensembl
chr6:138852747..138854692hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381946
hg191946
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572759
Supporting Variants
Samples
Known GenesNHSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272462
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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