A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569644



Internal ID20942715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137371318..137410651hg38UCSC Ensembl
chr3:137090160..137129493hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3839334
hg1939334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259696
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569644
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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