A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565056



Internal ID20938127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37325589..37326134hg38UCSC Ensembl
chr6:37293365..37293910hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270745
Samples
Known GenesTBC1D22B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565056
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