A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250679



Internal ID20817719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235052919..235058426hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385508
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547626
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250679
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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