A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545375



Internal ID20918606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21201117..21267465hg38UCSC Ensembl
chr3:21242609..21308957hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3866349
hg1966349
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261937
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545375
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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