A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573450



Internal ID20946521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96877088..96878659hg38UCSC Ensembl
chr5:96212792..96214363hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381572
hg191572
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267762
Samples
Known GenesERAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573450
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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