A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248660



Internal ID20815700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219082816..219088677hg38UCSC Ensembl
chr1:219256158..219262019hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg385862
hg195862
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538136
Supporting Variants
Samples
Known GenesLOC643723
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248660
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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