A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559799



Internal ID20932870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128013982..128015077hg38UCSC Ensembl
chr4:128935137..128936232hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg381096
hg191096
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263737
Samples
Known GenesC4orf29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559799
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