A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567253



Internal ID20940324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30781122..30782314hg38UCSC Ensembl
chr8:30638638..30639830hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381193
hg191193
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567253
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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