A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248552



Internal ID20815592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214071018..214071398hg38UCSC Ensembl
chr1:214244361..214244741hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544616
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248552
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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