A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264407



Internal ID20831447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169884150..169900046hg38UCSC Ensembl
chr4:170805301..170821197hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3815897
hg1915897
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569995
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264407
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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