A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546122



Internal ID20919341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32480225..32480321hg38UCSC Ensembl
chr3:32521717..32521813hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546122
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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