A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595937



Internal ID20969008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40655461..40656063hg38UCSC Ensembl
chr21:42027387..42027989hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254460
Samples
Known GenesDSCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595937
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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