A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562637



Internal ID20935708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136664718..136665575hg38UCSC Ensembl
chr6:136985856..136986713hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38858
hg19858
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6417n223
Supporting Variantsnssv18272395
Samples
Known GenesMAP3K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562637
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