A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271090



Internal ID20838130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121191544..121198036hg38UCSC Ensembl
chr6:121512690..121519182hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg386493
hg196493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561336
Supporting Variants
Samples
Known GenesTBC1D32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271090
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.01359


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