A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557137



Internal ID20930208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46887731..46888743hg38UCSC Ensembl
chr4:46889748..46890760hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg381013
hg191013
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5258n223
Supporting Variantsnssv18266335
Samples
Known GenesCOX7B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557137
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