A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569171



Internal ID20942242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38342733..38343033hg38UCSC Ensembl
chr8:38200251..38200551hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277921
Samples
Known GenesWHSC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569171
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