A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597822



Internal ID20970893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44886476..45014835hg38UCSC Ensembl
chr21:46306391..46434750hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38128360
hg19128360
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255093
Samples
Known GenesC21orf67, FAM207A, ITGB2, ITGB2-AS1, LINC00162, LINC00163
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597822
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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