A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597262



Internal ID20970333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33596662..33597093hg38UCSC Ensembl
chr21:34968968..34969399hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254054
Samples
Known GenesCRYZL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597262
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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