A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557971



Internal ID20931042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127278183..127279554hg38UCSC Ensembl
chr8:128290428..128291799hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg381372
hg191372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276216
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557971
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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