A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537436



Internal ID20910769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38166964..38168212hg38UCSC Ensembl
chr22:38562971..38564219hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381249
hg191249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073945
Samples
Known GenesPLA2G6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer