A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248664



Internal ID20815704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219375314..219375547hg38UCSC Ensembl
chr1:219548656..219548889hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542221
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248664
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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