A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549188



Internal ID20922356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31541487..31543094hg38UCSC Ensembl
chr3:31582979..31584586hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg381608
hg191608
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261356
Samples
Known GenesSTT3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549188
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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