A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564412



Internal ID20937483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67030509..67031397hg38UCSC Ensembl
chr8:67942744..67943632hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7375n223
Supporting Variantsnssv18278529
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564412
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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