A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250873



Internal ID20817913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32785192..32785643hg38UCSC Ensembl
chr1:33250793..33251244hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539610
Supporting Variants
Samples
Known GenesYARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250873
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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