A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575395



Internal ID20948466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30299964..30300934hg38UCSC Ensembl
chr8:30157480..30158450hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38971
hg19971
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575395
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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