A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265204



Internal ID20832244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39891134..39891794hg38UCSC Ensembl
chr4:39892754..39893414hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556129
Supporting Variants
Samples
Known GenesPDS5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265204
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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