A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259537



Internal ID20826577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:125448990..125449361hg38UCSC Ensembl
chr3:125167834..125168205hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566210
Supporting Variants
Samples
Known GenesSNX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259537
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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