A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559971



Internal ID20933042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101600965..101604106hg38UCSC Ensembl
chr7:101244245..101247386hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383142
hg193142
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272909
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559971
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