A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569001



Internal ID20942072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131239322..131240188hg38UCSC Ensembl
chr7:130924081..130924947hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271764
Samples
Known GenesMKLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569001
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