A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565589



Internal ID20938660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38519824..38521291hg38UCSC Ensembl
chr8:38377342..38378809hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg381468
hg191468
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277936
Samples
Known GenesC8orf86
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565589
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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