A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265565



Internal ID20832605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21784340..21800514hg38UCSC Ensembl
chr4:21785963..21802137hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3816175
hg1916175
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556858
Supporting Variants
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265565
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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