A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556536



Internal ID20929607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81643266..81644817hg38UCSC Ensembl
chr8:82555501..82557052hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381552
hg191552
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556536
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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