A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266733



Internal ID20833773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87950237..87950781hg38UCSC Ensembl
chr4:88871389..88871933hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560538
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266733
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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