A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561061



Internal ID20934132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70823820..70824199hg38UCSC Ensembl
chr4:71689537..71689916hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265968
Samples
Known GenesGRSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561061
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