A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564499



Internal ID20937570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97070750..97071181hg38UCSC Ensembl
chr5:96406454..96406885hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564499
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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