A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562482



Internal ID20935553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129165613..129166256hg38UCSC Ensembl
chr7:128805454..128806097hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273053
Samples
Known GenesTSPAN33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562482
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