A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262242



Internal ID20829282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62890837..62896324hg38UCSC Ensembl
chr3:62876512..62881999hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg385488
hg195488
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262242
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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