A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265646



Internal ID20832686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25537271..25538143hg38UCSC Ensembl
chr4:25538893..25539765hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265646
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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