A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568663



Internal ID20941734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85271986..85272485hg38UCSC Ensembl
chr8:86184215..86184714hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278907
Samples
Known GenesCA13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568663
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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