A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104571



Internal ID22013804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43262465..43335986hg38UCSC Ensembl
chr21:44682676..44755866hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3873522
hg1973191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638796
Samples
Known GenesLINC00322
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104571
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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