A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561368



Internal ID20934439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32959028..32960061hg38UCSC Ensembl
chr8:32816546..32817579hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381034
hg191034
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7312n223
Supporting Variantsnssv18277774
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561368
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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