A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572786



Internal ID20945857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129003435..129005620hg38UCSC Ensembl
chr3:128722278..128724463hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382186
hg192186
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259607
Samples
Known GenesEFCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572786
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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