A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564274



Internal ID20937345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161098252..161099893hg38UCSC Ensembl
chr6:161519284..161520925hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381642
hg191642
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269862
Samples
Known GenesMAP3K4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564274
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