A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253937



Internal ID20820977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85537475..85544007hg38UCSC Ensembl
chr1:86003158..86009690hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg386533
hg196533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536490
Supporting Variants
Samples
Known GenesDDAH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253937
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00013


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