A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263887



Internal ID20830927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153354555..153354990hg38UCSC Ensembl
chr4:154275707..154276142hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575001
Supporting Variants
Samples
Known GenesMND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263887
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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