A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561301



Internal ID20934372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96713162..96713697hg38UCSC Ensembl
chr5:96048866..96049401hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5821n223
Supporting Variantsnssv18267755
Samples
Known GenesCAST
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561301
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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