A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561543



Internal ID20934614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45599710..45600566hg38UCSC Ensembl
chr7:45639309..45640165hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276031
Samples
Known GenesADCY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561543
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