A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544446



Internal ID20917684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43057301..43092700hg38UCSC Ensembl
chr22:43453307..43488706hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3835400
hg1935400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074374
Samples
Known GenesTTLL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544446
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