A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557102



Internal ID20930173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86044073..86090124hg38UCSC Ensembl
chr7:85673389..85719440hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3846052
hg1946052
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557102
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