A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221161



Internal ID20788201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60624197..60624741hg38UCSC Ensembl
chr13:61198331..61198875hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576757
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221161
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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