A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218860



Internal ID20785900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32479066..32479330hg38UCSC Ensembl
chr13:33053203..33053467hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578659
Supporting Variants
Samples
Known GenesN4BP2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218860
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00023


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