A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560038



Internal ID20933109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:29998549..30004205hg38UCSC Ensembl
chr5:29998656..30004312hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg385657
hg195657
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269600
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560038
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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