A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569274



Internal ID20942345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158674143..158675097hg38UCSC Ensembl
chr3:158391932..158392886hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38955
hg19955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259808
Samples
Known GenesGFM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569274
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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