A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272593



Internal ID20839633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135191329..135192413hg38UCSC Ensembl
chr7:134876081..134877165hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381085
hg191085
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556416
Supporting Variants
Samples
Known GenesWDR91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272593
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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