A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269084



Internal ID20836124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55265221..55520270hg38UCSC Ensembl
chr5:54561049..54816098hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38255050
hg19255050
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570183
Supporting Variants
Samples
Known GenesDHX29, MIR5687, PPAP2A, SKIV2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269084
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0001


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