A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259473



Internal ID20826513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101583371..101583932hg38UCSC Ensembl
chr3:101302215..101302776hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537599
Supporting Variants
Samples
Known GenesPCNP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259473
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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