A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263189



Internal ID20830229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15018023..15019017hg38UCSC Ensembl
chr3:15059530..15060524hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545132
Supporting Variants
Samples
Known GenesNR2C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263189
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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