A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221112



Internal ID20788152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106866843..107288456hg38UCSC Ensembl
chr13:107519191..107940804hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38421614
hg19421614
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588247
Supporting Variants
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221112
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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