A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272111



Internal ID20839151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89607173..89607662hg38UCSC Ensembl
chr6:90316892..90317381hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564820
Supporting Variants
Samples
Known GenesANKRD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272111
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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