A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597772



Internal ID20970843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33741692..33742266hg38UCSC Ensembl
chr21:35113997..35114571hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254067
Samples
Known GenesITSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597772
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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