A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567786



Internal ID20940857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105103871..105104723hg38UCSC Ensembl
chr7:104744318..104745170hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38853
hg19853
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7043n223
Supporting Variantsnssv18272231
Samples
Known GenesKMT2E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567786
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