A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252962



Internal ID20820002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26062585..26062781hg38UCSC Ensembl
chr21:27434901..27435097hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597062
Supporting Variants
Samples
Known GenesAPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252962
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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