A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562320



Internal ID20935391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141589143..141589627hg38UCSC Ensembl
chr3:141307985..141308469hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259773
Samples
Known GenesRASA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562320
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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