A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268077



Internal ID20835117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163465355..163465864hg38UCSC Ensembl
chr5:162892361..162892870hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574789
Supporting Variants
Samples
Known GenesHMMR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268077
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0006


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