A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561276



Internal ID20934347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28770374..28772319hg38UCSC Ensembl
chr8:28627891..28629836hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg381946
hg191946
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277623
Samples
Known GenesINTS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561276
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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