A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265698



Internal ID20832738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44897306..44898489hg38UCSC Ensembl
chr4:44899323..44900506hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg381184
hg191184
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265698
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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