A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254230



Internal ID20821270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:21355200..21355705hg38UCSC Ensembl
chr21:22727520..22728025hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596453
Supporting Variants
Samples
Known GenesNCAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254230
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00019


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