A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561375



Internal ID20934446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172163135..172165172hg38UCSC Ensembl
chr3:171880925..171882962hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg382038
hg192038
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260546
Samples
Known GenesFNDC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561375
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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