A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559136



Internal ID20932207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151210625..151211707hg38UCSC Ensembl
chr5:150590186..150591268hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268709
Samples
Known GenesCCDC69
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559136
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