A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556028



Internal ID20929099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134650248..134655178hg38UCSC Ensembl
chr5:133985938..133990868hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg384931
hg194931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267328
Samples
Known GenesSEC24A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556028
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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