A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572370



Internal ID20945441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27010031..27010800hg38UCSC Ensembl
chr8:26867548..26868317hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572370
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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