A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267624



Internal ID20834664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169858740..169860003hg38UCSC Ensembl
chr5:169285744..169287007hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563514
Supporting Variants
Samples
Known GenesDOCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267624
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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