A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574903



Internal ID20947974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:71084756..71099056hg38UCSC Ensembl
chr8:71996991..72011291hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3814301
hg1914301
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer