A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599812



Internal ID20972883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33614082..33614716hg38UCSC Ensembl
chr21:34986388..34987022hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4593n223
Supporting Variantsnssv18254056
Samples
Known GenesCRYZL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599812
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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